Spina bifida is a birth defect that occurs when the spine and spinal cord don't form properly. It falls under the broader category of NTD (Neural Tube Defects).
Spina bifida is a birth defect where the spinal cord fails to close properly, leaving it exposed. There are three main types: spina bifida occulta, which has no protrusion and is usually asymptomatic; meningocele, which involves protrusion of meninges and cerebrospinal fluid in a sac; and myelomeningocele, the most severe form, which involves protrusion of meninges, spinal cord, and cerebrospinal fluid. Treatment involves surgery to close the defect as well as management of any related conditions like hydrocephalus or paralysis. Parents are counseled and trained to care for the child's lifelong medical needs.
This document discusses spina bifida, a neural tube defect caused by the incomplete development of the spinal cord and vertebrae. It describes the case of a newborn with a bulging cyst on his back, limited leg movement, and foot deformities, which are signs of spina bifida. The document defines and classifies spina bifida, discusses risk factors, associated conditions, treatment options, complications, prevention methods through folic acid supplementation, and prognosis.
Central nervous system defects include disorders caused by an imbalance of cerebrospinal fluid (as in hydrocephalus) and a range of disorders resulting from malformations of the neural tube during embryonic development (often called “neural tube defects”). These defects vary from mild to severely disabling.
Spina bifida is a birth defect where there is an incomplete closing of the backbone and membranes around the spinal cord. It is a developmental congenital anomaly
Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving an opening in the vertebrae. There are three main types - spina bifida occulta which has no symptoms, meningocele where only the meninges protrude out, and myelomeningocele where the meninges and spinal cord protrude out. Myelomeningocele is the most severe and can cause paralysis. Diagnosis is usually made prenatally through ultrasound or after birth upon visual inspection. Treatment involves surgery to close the opening soon after birth along with lifelong physical therapy and management of complications which commonly include hydrocephalus, learning disabilities, and bladder/bowel issues.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It occurs when the neural tube fails to close fully during early embryonic development. The most common type is myelomeningocele, where parts of the spinal cord and meninges protrude out of an opening in the spine. This can cause paralysis, loss of feeling, and problems with bladder and bowel control below the level of the defect. Treatment involves surgery to close the opening and manage any related complications like hydrocephalus. Prevention focuses on adequate folic acid intake before and during early pregnancy.
This document provides an overview of neural tube defects (NTDs), which are among the most common birth defects. It discusses the embryology, causes, types (including anencephaly and spina bifida), clinical presentation, diagnostic tests (such as ultrasound and MRI), and management (including prenatal surgery, medical care of newborns, and post-natal surgical repair). Key points covered include the importance of folic acid supplementation to prevent NTDs, the variety of potential genetic and environmental risk factors, and ongoing areas of research and debate around improving treatment and outcomes.
This document discusses neural tube defects, specifically spina bifida. It defines spina bifida as a birth defect involving incomplete development of the spinal cord or its coverings. There are two main types - spina bifida occulta, which is usually asymptomatic, and spina bifida manifesta, which includes meningocele (protrusion of meninges) and myelomeningocele (protrusion of meninges and spinal cord). Causes include genetic factors and folic acid deficiency. Symptoms depend on the type but may include bladder/bowel issues or developmental delays. Treatment involves surgery to repair the defect and address any related issues like hydrocephalus. Nursing care focuses on preventing infection, managing elimination
Spina bifida is a birth defect where the spinal cord fails to close properly, leaving it exposed. There are three main types: spina bifida occulta, which has no protrusion and is usually asymptomatic; meningocele, which involves protrusion of meninges and cerebrospinal fluid in a sac; and myelomeningocele, the most severe form, which involves protrusion of meninges, spinal cord, and cerebrospinal fluid. Treatment involves surgery to close the defect as well as management of any related conditions like hydrocephalus or paralysis. Parents are counseled and trained to care for the child's lifelong medical needs.
This document discusses spina bifida, a neural tube defect caused by the incomplete development of the spinal cord and vertebrae. It describes the case of a newborn with a bulging cyst on his back, limited leg movement, and foot deformities, which are signs of spina bifida. The document defines and classifies spina bifida, discusses risk factors, associated conditions, treatment options, complications, prevention methods through folic acid supplementation, and prognosis.
Central nervous system defects include disorders caused by an imbalance of cerebrospinal fluid (as in hydrocephalus) and a range of disorders resulting from malformations of the neural tube during embryonic development (often called “neural tube defects”). These defects vary from mild to severely disabling.
Spina bifida is a birth defect where there is an incomplete closing of the backbone and membranes around the spinal cord. It is a developmental congenital anomaly
Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving an opening in the vertebrae. There are three main types - spina bifida occulta which has no symptoms, meningocele where only the meninges protrude out, and myelomeningocele where the meninges and spinal cord protrude out. Myelomeningocele is the most severe and can cause paralysis. Diagnosis is usually made prenatally through ultrasound or after birth upon visual inspection. Treatment involves surgery to close the opening soon after birth along with lifelong physical therapy and management of complications which commonly include hydrocephalus, learning disabilities, and bladder/bowel issues.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It occurs when the neural tube fails to close fully during early embryonic development. The most common type is myelomeningocele, where parts of the spinal cord and meninges protrude out of an opening in the spine. This can cause paralysis, loss of feeling, and problems with bladder and bowel control below the level of the defect. Treatment involves surgery to close the opening and manage any related complications like hydrocephalus. Prevention focuses on adequate folic acid intake before and during early pregnancy.
This document provides an overview of neural tube defects (NTDs), which are among the most common birth defects. It discusses the embryology, causes, types (including anencephaly and spina bifida), clinical presentation, diagnostic tests (such as ultrasound and MRI), and management (including prenatal surgery, medical care of newborns, and post-natal surgical repair). Key points covered include the importance of folic acid supplementation to prevent NTDs, the variety of potential genetic and environmental risk factors, and ongoing areas of research and debate around improving treatment and outcomes.
This document discusses neural tube defects, specifically spina bifida. It defines spina bifida as a birth defect involving incomplete development of the spinal cord or its coverings. There are two main types - spina bifida occulta, which is usually asymptomatic, and spina bifida manifesta, which includes meningocele (protrusion of meninges) and myelomeningocele (protrusion of meninges and spinal cord). Causes include genetic factors and folic acid deficiency. Symptoms depend on the type but may include bladder/bowel issues or developmental delays. Treatment involves surgery to repair the defect and address any related issues like hydrocephalus. Nursing care focuses on preventing infection, managing elimination
Neural tube defects occur when the neural tube fails to close properly during early embryonic development, leaving an opening in the spine or skull. The most common type is spina bifida, where a split forms in the spine. Spina bifida can range from mild (occulta) where there is a small defect but no problems, to more severe forms (meningocele and myelomeningocele) where the spinal cord or membranes may protrude out and cause paralysis and bowel/bladder issues. Risk factors include low folic acid, diabetes, and seizures. Treatment involves surgery soon after birth to cover the opening and manage complications like hydrocephalus. Lifelong management focuses on rehabilitation, prevention of injury and infection, and
Clubfoot is a birth defect where the foot is twisted into an abnormal position. It occurs in about 1 in 1,000 births and is more common in males. The cause is unknown but may involve abnormal foot positioning in the uterus. Treatment involves application of casts or use of splints to manipulate the foot into a corrected position.
This document provides information on congenital muscular torticollis and its treatment. It describes how congenital muscular torticollis is caused by fibromatosis in the sternocleidomastoid muscle. Conservative treatment including stretching is recommended during infancy. Surgery may be needed if deformity persists beyond age 1. The goal of surgery before age 6-8 is to allow remodeling and prevent facial asymmetry.
Rickets is a softening of the bones due to vitamin D deficiency which impairs the absorption of calcium and phosphorus. It can cause skeletal deformities like bowed legs. Risk factors include dark skin, lack of sunlight exposure, and exclusive breastfeeding without vitamin D supplements. Symptoms include impaired growth and bone or muscle pain. Treatment involves adding vitamin D, calcium, and sunlight exposure to the diet.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It can range from mild to severe, causing physical and intellectual disabilities. It occurs when the neural tube fails to close fully during early embryonic development. The three main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves surgery to repair the spine and prevent infection, along with physical therapy, bladder and bowel management, and orthopedic care. Prevention focuses on adequate folic acid intake before and during pregnancy to help reduce risks.
This document summarizes the development of the central nervous system during the 4th week of gestation. It describes how the neural groove deepens and closes to form the neural tube. Cells within the neural tube then differentiate into neuroblasts and neurons. The meninges develop from surrounding mesenchyme. Vertebral bodies form around the notochord and projections extend around the neural canal to form the vertebral arches. Failure of these arches to fuse can result in spina bifida. The document further describes the types and causes of spina bifida and approaches to management.
Spina bifida is a birth defect where the spinal column does not fully close around the spinal cord. It can range from mild to severe depending on the location and severity of the opening. The main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves early surgery, physical/occupational therapy, bracing, and management of any neurological problems or secondary issues like hydrocephalus. Taking adequate folic acid before and during pregnancy can help prevent spina bifida in future children.
Club foot, also known as congenital talipes equinovarus, is a congenital deformity where the foot is twisted out of shape. It occurs in approximately 1 in 1,000 live births. While the exact cause is unknown, risk factors include family history, smoking during pregnancy, and lack of amniotic fluid. Treatment options for club foot include stretching and casting, which is the most common approach, as well as stretching and taping or surgery. With early treatment, those with club foot can often walk normally and lead active lives.
Cerebral palsy is an umbrella term for physical disabilities caused by damage to the brain before or at birth. It is characterized by impaired muscle coordination and other disabilities. The prevalence is about 4 per 1000 live births. There are several types classified by motor deficit, including spastic (the most common), dyskinetic, atonic, and mixed forms. Management involves medical treatment to alleviate symptoms, physical and occupational therapy, and sometimes surgery to correct issues like scoliosis.
The document discusses different types of spinal curvature abnormalities including kyphosis, lordosis, and scoliosis. It defines each condition and describes their causes, symptoms, diagnostic tests, and treatment options. There are three main types of kyphosis - postural, Scheuermann's, and congenital. Lordosis is an inward curvature of the lumbar or cervical spine that can be caused by factors like poor posture or congenital abnormalities. Scoliosis is a lateral curvature of the spine that can be idiopathic, congenital, or neuromuscular in origin. Treatment depends on the underlying cause but may include exercises, bracing, or corrective surgery.
This document discusses congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births. Clubfoot is usually an isolated problem in otherwise healthy newborns and is twice as common in males. Treatment typically begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper use of braces after treatment is needed to prevent the foot from returning to its original position. The cause is usually unknown but genetics and environmental factors may play a role. Nursing care focuses on supporting parents, educating on treatment and self-care, and protecting the skin during casting.
Spina bifida is a birth defect where the spine and spinal cord do not form properly, leaving an opening in the spine. It occurs in about 1-2 per 1000 live births. There are three main types: spina bifida occulta which has no symptoms, meningocele which is a sac protruding from the spine containing fluid and membranes, and myelomeningocele which is the most severe form where the spinal cord and membranes protrude out. Treatment depends on the type but may include surgery to close the opening after birth along with management to prevent infections and complications.
This document discusses spina bifida, including:
- Defining spina bifida as an incomplete closure of the neural tube, usually in the lumbar or sacral region.
- Describing the different types from spina bifida occulta to myelomeningocele.
- Detailing the various clinical presentations depending on the location and severity, including neurological deficits, hydrocephalus, orthopedic issues.
- Explaining that treatment involves surgery to cover or untether the spinal cord, along with medications, physical/occupational therapy, and follow-up to address complications.
- Emphasizing prevention through adequate folate intake before and during pregnancy to reduce the risk of spina bifida
Spina Bifida: Physiotherapy in the management of meningomyeloceleAyobami Ayodele
Spina bifida is a treatable spinal cord malformation that occurs in varying degrees of severity. Meningomyelocele is associated with abnormal development of the cranial neural tube, which results in several characteristic CNS anomalies. About 90% of babies born with Spina Bifida now live to be adults, about 80% have normal intelligence and about 75% play sports and do other fun activities. Most do well in school, and many play in sports.
The document discusses Spinal Bifida, beginning with the group members presenting and objectives of the presentation. It defines Spinal Bifida as a birth defect involving failure of vertebral arch fusion. It describes the types (Occulta, Cystica with Meningocele and Myelomeningocele forms) and discusses etiology, pathophysiology, clinical manifestations, diagnostic tests, medical and nursing management, and complications of Spinal Bifida. The presentation aims to provide knowledge on Spinal Bifida and its characteristics to students.
The document discusses various reflexes seen in infants and their significance. It begins by defining a reflex and describing the basic reflex arc involving receptors, afferent nerves, centers, efferent nerves and effectors. Reflexes are then classified based on whether they are inborn or acquired, their neurological pathway, purpose and clinical presentation. Several important reflexes seen in newborns like the moro, rooting and babinski reflexes are explained in detail. The document emphasizes that assessment of infant reflexes helps identify normal development and potential abnormalities.
Spina Bifida Birth Defects: Possible Causes of Congenital Injuries Exploredlawsuitlegal
What causes spina bifida? The following examines the data for and against an antidepressant (SSRI) causal link for congenital spina bifida and other malformations in newborns. We gathered some of the important research studies and shared their findings.
Allegations have been made that a number of developmental problems and congenital injuries are caused by prenatal SSRI exposure. Are these drugs dangerous or is it just tort attorneys looking for big pockets.
Our spina bifida lawyers are investigating claims from families whose babies were born with complications. If your child was exposed in utero to an anti-depressant, and was born with a congenital defect, visit our site and share what happened immediately to get more information on possible lawsuit options which may be available.
Encephaloceles are rare birth defects associated with skull defects characterized by partial lacking of bone fusion leaving a gap through which a portion of the brain sticks out (protrudes).
MYELOMENINGOCELE copy.pptx a slide describing the conditionAjisafeZainab
Myelomeningocele is a disorder of the nervous system particularly the spine and spinal cord, before we go further in this presentation there are some terms to know to aid understanding.
➢Neural tube; The neural tube forms the early brain and spine, As development progresses, the top of the neural tube becomes the brain, and the rest of the tube becomes the spinal cord. An NTD happens when this tube doesn't close completely somewhere along its length. Neural tube closure is completed 28 days (four weeks) from conception.
➢Alpha fetoprotein; AFP is a protein that the liver makes when its cells are growing and dividing to make new cells. AFP is normally high in unborn babies. After birth, AFP levels drop very low. Healthy children and adults who aren't pregnant have very little AFP in their blood. Maternal AFP serum level is used to screen for Down syndrome, neural tube defects, and other chromosomal abnormalities.
➢Spinal bifida; Spina bifida is a condition that affects the spine and is usually apparent at birth. It is a type of neural tube defect (NTD).
Nursing management of myelomeningocele
Types of spinal Bifida
Pathophysiology of myelomeningocele
Spina bifida is a birth disorder that involves the incomplete development of the spine. In the first month of pregnancy, a special set of cells forms the “neural tube;” the top of the tube becomes the brain, and the remainder becomes the spinal cord and structures around it. In spina bifida, the neural tube doesn’t close completely and some of the bones of the spine do not close in the back. This can result in an opening anywhere along the spine and may cause damage to the spinal cord and nerves.There are four types of spina bifida: occulta, closed neural tube defects, meningocele, and myelomeningocele. The symptoms of spina bifida vary from person to person, depending on the type and level of involvement. Most cases are mild and do not require special treatment. The more serious cases involve nerve damage.
Occulta is the mildest and most common form in which one or more bones of the spinal column (vertebrae) are malformed. The name “occulta,” which means “hidden,” indicates that a layer of skin covers the opening in the bones of the spine. It usually shows no symptoms and is often found by accident on an x-ray or similar test.
Closed neural tube defects are a diverse group of disorders in which the spine may have malformations of fat, bone, or the membranes (the meninges) that cover the spinal cord. Many of these neural tube defects require surgery in childhood. People with this type of spina bifida may have weakness of the legs and trouble with bowel and bladder control. These issues may change or progress as children grow. It is important to have close communication with doctors to minimize these changes as much as possible.
Meningocele occurs when the meninges protrude through the spine and cause a sac of spinal fluid on the back. This fluid is typically only around the brain and spine, but a problem with the bony covering over the spine allows it to poke out. The malformation contains no nerves and may or may not be covered by a layer of skin. Individuals with meningocele may have minor symptoms.Myelomeningocele is the most severe form of spina bifida. A portion of the spinal cord or nerves are exposed in a sac through an opening in the spine that may or may not be covered by the meninges. The opening can be closed surgically while the baby is in utero or shortly after the baby is born. Most people with myelomeningocele experience changes in brain structure, leg weakness, and bladder and bowel dysfunction.
Myelomeningocele is often called a "snowflake condition" because no two people with the condition are the same. Typically, if the opening in the spine is lower down the back, the person will experience less symptoms. People with myelomeningocele require close follow-up with physicians throughout their childhood and lifespan to maximize their function and prevent complications like kidney failure.Complications of spina bifida may include:
Abnormal sensation or paralysis, which mostly occurs with closed neural tube defects and myelomenin
Neural tube defects occur when the neural tube fails to close properly during early embryonic development, leaving an opening in the spine or skull. The most common type is spina bifida, where a split forms in the spine. Spina bifida can range from mild (occulta) where there is a small defect but no problems, to more severe forms (meningocele and myelomeningocele) where the spinal cord or membranes may protrude out and cause paralysis and bowel/bladder issues. Risk factors include low folic acid, diabetes, and seizures. Treatment involves surgery soon after birth to cover the opening and manage complications like hydrocephalus. Lifelong management focuses on rehabilitation, prevention of injury and infection, and
Clubfoot is a birth defect where the foot is twisted into an abnormal position. It occurs in about 1 in 1,000 births and is more common in males. The cause is unknown but may involve abnormal foot positioning in the uterus. Treatment involves application of casts or use of splints to manipulate the foot into a corrected position.
This document provides information on congenital muscular torticollis and its treatment. It describes how congenital muscular torticollis is caused by fibromatosis in the sternocleidomastoid muscle. Conservative treatment including stretching is recommended during infancy. Surgery may be needed if deformity persists beyond age 1. The goal of surgery before age 6-8 is to allow remodeling and prevent facial asymmetry.
Rickets is a softening of the bones due to vitamin D deficiency which impairs the absorption of calcium and phosphorus. It can cause skeletal deformities like bowed legs. Risk factors include dark skin, lack of sunlight exposure, and exclusive breastfeeding without vitamin D supplements. Symptoms include impaired growth and bone or muscle pain. Treatment involves adding vitamin D, calcium, and sunlight exposure to the diet.
Spina bifida is a birth defect where the spine and spinal cord do not form properly. It can range from mild to severe, causing physical and intellectual disabilities. It occurs when the neural tube fails to close fully during early embryonic development. The three main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves surgery to repair the spine and prevent infection, along with physical therapy, bladder and bowel management, and orthopedic care. Prevention focuses on adequate folic acid intake before and during pregnancy to help reduce risks.
This document summarizes the development of the central nervous system during the 4th week of gestation. It describes how the neural groove deepens and closes to form the neural tube. Cells within the neural tube then differentiate into neuroblasts and neurons. The meninges develop from surrounding mesenchyme. Vertebral bodies form around the notochord and projections extend around the neural canal to form the vertebral arches. Failure of these arches to fuse can result in spina bifida. The document further describes the types and causes of spina bifida and approaches to management.
Spina bifida is a birth defect where the spinal column does not fully close around the spinal cord. It can range from mild to severe depending on the location and severity of the opening. The main types are spina bifida occulta, meningocele, and myelomeningocele. Treatment involves early surgery, physical/occupational therapy, bracing, and management of any neurological problems or secondary issues like hydrocephalus. Taking adequate folic acid before and during pregnancy can help prevent spina bifida in future children.
Club foot, also known as congenital talipes equinovarus, is a congenital deformity where the foot is twisted out of shape. It occurs in approximately 1 in 1,000 live births. While the exact cause is unknown, risk factors include family history, smoking during pregnancy, and lack of amniotic fluid. Treatment options for club foot include stretching and casting, which is the most common approach, as well as stretching and taping or surgery. With early treatment, those with club foot can often walk normally and lead active lives.
Cerebral palsy is an umbrella term for physical disabilities caused by damage to the brain before or at birth. It is characterized by impaired muscle coordination and other disabilities. The prevalence is about 4 per 1000 live births. There are several types classified by motor deficit, including spastic (the most common), dyskinetic, atonic, and mixed forms. Management involves medical treatment to alleviate symptoms, physical and occupational therapy, and sometimes surgery to correct issues like scoliosis.
The document discusses different types of spinal curvature abnormalities including kyphosis, lordosis, and scoliosis. It defines each condition and describes their causes, symptoms, diagnostic tests, and treatment options. There are three main types of kyphosis - postural, Scheuermann's, and congenital. Lordosis is an inward curvature of the lumbar or cervical spine that can be caused by factors like poor posture or congenital abnormalities. Scoliosis is a lateral curvature of the spine that can be idiopathic, congenital, or neuromuscular in origin. Treatment depends on the underlying cause but may include exercises, bracing, or corrective surgery.
This document discusses congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births. Clubfoot is usually an isolated problem in otherwise healthy newborns and is twice as common in males. Treatment typically begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper use of braces after treatment is needed to prevent the foot from returning to its original position. The cause is usually unknown but genetics and environmental factors may play a role. Nursing care focuses on supporting parents, educating on treatment and self-care, and protecting the skin during casting.
Spina bifida is a birth defect where the spine and spinal cord do not form properly, leaving an opening in the spine. It occurs in about 1-2 per 1000 live births. There are three main types: spina bifida occulta which has no symptoms, meningocele which is a sac protruding from the spine containing fluid and membranes, and myelomeningocele which is the most severe form where the spinal cord and membranes protrude out. Treatment depends on the type but may include surgery to close the opening after birth along with management to prevent infections and complications.
This document discusses spina bifida, including:
- Defining spina bifida as an incomplete closure of the neural tube, usually in the lumbar or sacral region.
- Describing the different types from spina bifida occulta to myelomeningocele.
- Detailing the various clinical presentations depending on the location and severity, including neurological deficits, hydrocephalus, orthopedic issues.
- Explaining that treatment involves surgery to cover or untether the spinal cord, along with medications, physical/occupational therapy, and follow-up to address complications.
- Emphasizing prevention through adequate folate intake before and during pregnancy to reduce the risk of spina bifida
Spina Bifida: Physiotherapy in the management of meningomyeloceleAyobami Ayodele
Spina bifida is a treatable spinal cord malformation that occurs in varying degrees of severity. Meningomyelocele is associated with abnormal development of the cranial neural tube, which results in several characteristic CNS anomalies. About 90% of babies born with Spina Bifida now live to be adults, about 80% have normal intelligence and about 75% play sports and do other fun activities. Most do well in school, and many play in sports.
The document discusses Spinal Bifida, beginning with the group members presenting and objectives of the presentation. It defines Spinal Bifida as a birth defect involving failure of vertebral arch fusion. It describes the types (Occulta, Cystica with Meningocele and Myelomeningocele forms) and discusses etiology, pathophysiology, clinical manifestations, diagnostic tests, medical and nursing management, and complications of Spinal Bifida. The presentation aims to provide knowledge on Spinal Bifida and its characteristics to students.
The document discusses various reflexes seen in infants and their significance. It begins by defining a reflex and describing the basic reflex arc involving receptors, afferent nerves, centers, efferent nerves and effectors. Reflexes are then classified based on whether they are inborn or acquired, their neurological pathway, purpose and clinical presentation. Several important reflexes seen in newborns like the moro, rooting and babinski reflexes are explained in detail. The document emphasizes that assessment of infant reflexes helps identify normal development and potential abnormalities.
Spina Bifida Birth Defects: Possible Causes of Congenital Injuries Exploredlawsuitlegal
What causes spina bifida? The following examines the data for and against an antidepressant (SSRI) causal link for congenital spina bifida and other malformations in newborns. We gathered some of the important research studies and shared their findings.
Allegations have been made that a number of developmental problems and congenital injuries are caused by prenatal SSRI exposure. Are these drugs dangerous or is it just tort attorneys looking for big pockets.
Our spina bifida lawyers are investigating claims from families whose babies were born with complications. If your child was exposed in utero to an anti-depressant, and was born with a congenital defect, visit our site and share what happened immediately to get more information on possible lawsuit options which may be available.
Encephaloceles are rare birth defects associated with skull defects characterized by partial lacking of bone fusion leaving a gap through which a portion of the brain sticks out (protrudes).
MYELOMENINGOCELE copy.pptx a slide describing the conditionAjisafeZainab
Myelomeningocele is a disorder of the nervous system particularly the spine and spinal cord, before we go further in this presentation there are some terms to know to aid understanding.
➢Neural tube; The neural tube forms the early brain and spine, As development progresses, the top of the neural tube becomes the brain, and the rest of the tube becomes the spinal cord. An NTD happens when this tube doesn't close completely somewhere along its length. Neural tube closure is completed 28 days (four weeks) from conception.
➢Alpha fetoprotein; AFP is a protein that the liver makes when its cells are growing and dividing to make new cells. AFP is normally high in unborn babies. After birth, AFP levels drop very low. Healthy children and adults who aren't pregnant have very little AFP in their blood. Maternal AFP serum level is used to screen for Down syndrome, neural tube defects, and other chromosomal abnormalities.
➢Spinal bifida; Spina bifida is a condition that affects the spine and is usually apparent at birth. It is a type of neural tube defect (NTD).
Nursing management of myelomeningocele
Types of spinal Bifida
Pathophysiology of myelomeningocele
Spina bifida is a birth disorder that involves the incomplete development of the spine. In the first month of pregnancy, a special set of cells forms the “neural tube;” the top of the tube becomes the brain, and the remainder becomes the spinal cord and structures around it. In spina bifida, the neural tube doesn’t close completely and some of the bones of the spine do not close in the back. This can result in an opening anywhere along the spine and may cause damage to the spinal cord and nerves.There are four types of spina bifida: occulta, closed neural tube defects, meningocele, and myelomeningocele. The symptoms of spina bifida vary from person to person, depending on the type and level of involvement. Most cases are mild and do not require special treatment. The more serious cases involve nerve damage.
Occulta is the mildest and most common form in which one or more bones of the spinal column (vertebrae) are malformed. The name “occulta,” which means “hidden,” indicates that a layer of skin covers the opening in the bones of the spine. It usually shows no symptoms and is often found by accident on an x-ray or similar test.
Closed neural tube defects are a diverse group of disorders in which the spine may have malformations of fat, bone, or the membranes (the meninges) that cover the spinal cord. Many of these neural tube defects require surgery in childhood. People with this type of spina bifida may have weakness of the legs and trouble with bowel and bladder control. These issues may change or progress as children grow. It is important to have close communication with doctors to minimize these changes as much as possible.
Meningocele occurs when the meninges protrude through the spine and cause a sac of spinal fluid on the back. This fluid is typically only around the brain and spine, but a problem with the bony covering over the spine allows it to poke out. The malformation contains no nerves and may or may not be covered by a layer of skin. Individuals with meningocele may have minor symptoms.Myelomeningocele is the most severe form of spina bifida. A portion of the spinal cord or nerves are exposed in a sac through an opening in the spine that may or may not be covered by the meninges. The opening can be closed surgically while the baby is in utero or shortly after the baby is born. Most people with myelomeningocele experience changes in brain structure, leg weakness, and bladder and bowel dysfunction.
Myelomeningocele is often called a "snowflake condition" because no two people with the condition are the same. Typically, if the opening in the spine is lower down the back, the person will experience less symptoms. People with myelomeningocele require close follow-up with physicians throughout their childhood and lifespan to maximize their function and prevent complications like kidney failure.Complications of spina bifida may include:
Abnormal sensation or paralysis, which mostly occurs with closed neural tube defects and myelomenin
Spina bifida is a birth defect where the spinal column does not fully close around the spinal cord. It occurs when the neural tube fails to close properly during early embryonic development. The main types are spina bifida occulta (mildest), meningocele (meninges protrude through opening), and myelomeningocele (most severe where spinal cord and membranes protrude). Symptoms range from minor skin marks to paralysis depending on location and severity of the defect. Treatment involves surgery to cover the exposed tissues and may include shunts to drain excess cerebrospinal fluid. Lifelong management focuses on rehabilitation, prevention of infections and complications, and addressing mobility, bladder, and bowel issues.
Spina bifida is a birth defect where the backbone and spinal canal do not close before birth, causing part of the spinal cord to protrude out of the back. It affects around 1 in 800 infants and can range from a mild condition where the spine does not fully close to more severe cases where parts of the spinal cord and membranes protrude out. Symptoms include issues with bladder/bowel control, paralysis, and hydrocephalus in many cases. Prenatal screening and folic acid supplementation can help reduce risks, while surgery after birth and lifelong treatment can address symptoms and complications.
Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving an opening in the vertebrae. It occurs when the neural tube fails to close fully during early embryonic development. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. Myelomeningocele is the most severe form and often results in paralysis and loss of sensation below the level of the defect. Risk factors include family history, obesity, fever during early pregnancy, and folic acid deficiency. Treatment involves surgery to close the opening and address any related issues like hydrocephalus. Lifelong management focuses on rehabilitation, preventing infections and complications, and addressing issues with mobility,
Meningomyelocele, also commonly known as myelomeningocele, is the most serious form of spina bifida. Spina bifida is a birth defect in which the spinal canal and the backbone don’t close before the baby is born. Check out this video to know more about Meningomyelocele!
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This document discusses Spina Bifida, a birth defect where the spine and spinal cord do not fully develop. It describes the different types including Occulta, Closed neural tube defects, Meningocele, and Myelomeningocele. Risk factors include family history, folic acid deficiency, diabetes, and obesity. Treatment depends on the type and severity but may include surgery to close the defect, shunts to drain fluid from the brain, and physical therapy. Taking 400 micrograms of folic acid daily can help prevent Spina Bifida.
My name is Dahianara Moran and I believe being the parent of a child with Spina Bifida is like having a sixth sense, something like a Super Mom. We learn quickly how to defend our little ones from the awkward moments, but most important, we come to enjoy the little things, value our moments, and commit to change the way the world defines “Disability”.
(1) Spina bifida is a birth defect where part of the spinal cord and its meninges are exposed through an opening in the backbone. (2) It results from the neural tube failing to close properly during early pregnancy. (3) Spina bifida can range from mild to severe depending on factors like the size and location of the defect and presence of complications such as hydrocephalus or Chiari malformation.
Spina bifida is a neural tube defect where the backbone does not fully close around the spinal cord during embryonic development. It can cause damage to the spinal cord and nerves. The main types are myelomeningocele, meningocele, and spina bifida occulta. Myelomeningocele is the most severe type, often causing mobility and bladder issues. Spina bifida is diagnosed through prenatal tests like ultrasound and AFP levels and treated after birth through surgery. Taking folic acid before and during pregnancy can help prevent spina bifida.
Neural tube defects are the most common congenital abnormality in India which can be easily prevented with due information and better nursing practices. Neural Tube Defects can be prevented with intake of folic acid.
Spina bifida is a neural tube defect where there is an incomplete closure of the vertebrae and neural tube. It can range from mild forms where there are no symptoms to more severe forms with neurological deficits depending on the location and severity of the defect. Management involves surgery to close the defect early in life as well as lifelong multidisciplinary care to address issues like bowel and bladder dysfunction, mobility, skin integrity, and neurodevelopment. Hydrocephalus is an excess of cerebrospinal fluid in the brain that can be congenital or acquired and may require surgical treatment like shunt placement to drain the fluid.
Congenital disorders, also known as birth defects, occur during fetal development and result in structural or functional anomalies. An estimated 6% of babies worldwide are born with a congenital disorder. Spina bifida is a birth defect that causes the backbone to not form properly, potentially damaging the spinal cord and nerves. It ranges in severity from spina bifida occulta, which has a hidden spine defect but normal nerves, to myelomeningocele, the most severe type in which the meninges and spinal nerves protrude out of the back through an opening in the spine. Prevention focuses on adequate prenatal folic acid intake by the mother. Treatment involves surgical repair and multidisciplinary care.
Spina bifida is a condition that affects the spine and is usually apparent at birth. It is a type of neural tube defect (NTD). Spina bifida can happen anywhere along the spine if the neural tube does not close all the way.
All about Spina Bifida:
Definition
7 Types
Causes
Health Status
Incidence and epidemiology
Prevention
Social impact
Management
Detection
Diagnosis
Treatment
Antibiotics
Careful observation
Physical therapy
This document discusses neural tube defects (NTDs), which occur early in pregnancy when the neural tubes fail to close properly. It describes different types of NTDs including spina bifida, anencephaly, and exencephaly. Spina bifida can be occulta, cystica, or myelomeningocele depending on whether the spinal cord or meninges protrude out. Anencephaly and exencephaly involve failure of the cranial neural tube to close. Risk factors include genetics and lack of folic acid. Prenatal screening can detect some NTDs but early fetal surgery is also being studied. Taking folic acid before and during pregnancy can help prevent NTDs.
The neural tube is the embryonic precursor to the central nervous system. During development, the neural tube forms as the neural folds lift and fuse together. Improper closure of openings in the neural tube can cause neural tube defects like anencephaly or spina bifida. Anencephaly involves failure of the brain and skull to develop properly. Spina bifida occurs when the spinal cord, brain, or their protective coverings do not fully develop, and can range from mild to severe depending on the type and extent of involvement. Treatment options depend on the specific type and symptoms of each defect.
Spinabifidia, also known as spina bifida, is a birth defect where the spine and spinal cord do not properly develop. It can range in severity from a mild form where there are no symptoms to a more severe form where the spinal cord and membranes protrude out of the open spine. Children with more severe forms may experience paralysis, nerve damage, and other issues. Early intervention and treatment is important to help support development and manage complications. Parents and teachers play an important role in caring for and educating children with spinabifidia.
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3. INDEX
INTRODUCTION
WHAT IS SPINA BIFIDA?
TYPES
ANATOMY REVIEW
NORMAL BAY VS MYELOMENINGOCELE BABY.
SYMPTOMS
COMPLICATION
CAUSES
PREVENTION
RISK FACTORS
PATHOPHYSIOLOHY
DIAGNOSIS
CLINICAL TRIALS
IMMEDIATE CARE
TREATMENTS
LIFE LONG TREATMENT
SOCIAL IMPACT
CONCULATION
REFERANCE
4. INTRODUCTION
Spina bifida is a birth defect that occurs
when the spine and spinal cord don't form
properly.
It falls under the broader category of NTD
(Neural Tube Defects).
The neural tube is the structure in the
developing embryo that gives rise to the
brain and spinal cord.
5. Cont…
Normally, the neural tube forms early
in pregnancy, and it closes by the 28th
day after conception.
In babies with spina bifida, a portion of
the neural tube fails to develop or
close properly, causing defects in the
spinal cord and in the bones of the
spine.
6. Cont..
Spina bifida is a relatively common
birth defect in U.S.
About 1,500 to 2,000 babies of the
4 million born in the United States
(U.S.) each year.
In India there are 5-7 cases per
1000 births.
7. What is Spina Bifida ?
Spina bifida also called split spine.
The words literally mean "split spine" in Latin.
A birth defect that occurs when the spine and
spinal cord don't form properly.
8. TYPES OF SPINA BIFIDA
The three most common types of spina
bifida are :
01 Spina Bifida Occulta.
02. Meningocele.
03. Myelomeningocele.
10. 01.Spina Bifida Occulta
Spina bifida occulta is the
mildest type of spina bifida.
It is sometimes called
“hidden” spina bifida. With
it, there is a small gap in the
spine, but no opening or sac
on the back.
The spinal cord and the
nerves usually are normal.
11. Cont…
Many times, spina bifida occulta is not
discovered until late childhood or
adulthood.
This type of spina bifida usually does
not cause any disabilities.
There is a dimple, hairy patch, dark
spot or birthmark over affected area.
No treatment needed.
12. 02. Meningocele
Another type of spina bifida is
meningocele.
With meningocele a sac of fluid
comes through an opening in the
baby’s back. But, the spinal cord is
not in this sac.
There is usually little or no nerve
damage.
This type of spina bifida can cause
minor disabilities.
13. 03. Myelomeningocele
Myelomeningocele is the most
serious type of spina bifida.
With this condition, a sac of
fluid comes through an
opening in the baby’s back.
This type of spina bifida
causes moderate to severe
disabilities,
14. Cont…
such as problems affecting how
the person goes to the
bathroom, loss of feeling in
the person’s legs or feet, and
not being able to move the
legs.
16. SYMPTOMS
Signs and symptoms of spina bifida vary by
type and severity. Symptoms can also differ
for each person.
Spina bifida occulta.
Many cases of SBO are very mild. When
symptoms occur, they generally include:
o Back pain
o Leg weakness
o Pain in the back of the legs
17. Cont..
o Loss of bladder or bowel control
o Scoliosis, or a curving of the spine
o Numbness in the back or legs
o Misshapen legs and feet
Sometimes there are visible signs
that a spinal cord abnormality, like SBO,
may be present.
o Hairy patch
o Discoloring or birthmark
o Dimple or indent
o Growth or pad of fat
18. Cont…
Meningocele.
The membranes around the spinal cord push out
through an opening in the vertebrae, forming a sac
filled with fluid, but this sac doesn't include the spinal
cord.
Myelomeningocele.
In this severe form of spina bifida:
The spinal canal remains open along several vertebrae
in the lower or middle back.
Both the membranes and the spinal cord or nerves
protrude at birth, forming a sac.
Tissues and nerves usually are exposed, though
sometimes skin covers the sac.
19. Cont…
Others:
Bladder and bowel problems (incontinence)
Sexual dysfunction.
Weakness and loss of sensation below the
defect.
Weakness of limbs.
Paralysis.
Orthopedic problems- scoliosis, clubfoot,
hip dislocation.
21. COMPLICATIONS
o Poor ability to walk.
o Problems with bladder or bowel
control.
o Hydrocephalus
o Tethered spinal cord.
o Latex allergy.
22. CAUSES
The exact cause of spina bifida remains a
mystery. No one knows what disrupts
complete closure of the neural tube,
causing this malformation to develop.
Scientists suspect the factors that cause
spina bifida are multiple:
o Genetic,
o Nutritional, and
o Environmental factors all play a role.
23. Cont…
Research studies indicate that
insufficient intake of folic acid—a
common B vitamin—in the mother’s
diet is a key factor in causing spina
bifida and other neural tube
defects.
Prenatal vitamins typically contain
folic acid as well as other vitamins.
24. PREVENTION
Since the causes of spina bifida is unknown,it is
difficult to prevent it, but folic acid and tests
during pregnancy can help.
If you are pregnant or could get pregnant, use the
following tips to help prevent your baby from having
spina bifida:
Take 400 micrograms (mcg) of folic acid every day.
If you have already had a pregnancy affected by
spina bifida, you may need to take a higher dose
of folic acid before pregnancy and during early
pregnancy.
25. Talk to your doctor to discuss
what’s best for you.
Talk to your doctor or pharmacist
about any prescription and over-
the counter drugs, vitamins, and
dietary or herbal supplements you
are taking.
26. RISK FACTORS
Spina bifida is more common among
whites and Hispanics, and females are
affected more often than males.
They have identified some risk factors:
Folate deficiency:
Folate (vitamin B-9) is important to the
healthy development of a baby. Folate is
the natural form of vitamin B-9.
27. Cont…
Some medications:
For example, anti-seizure medications,
such as valproic acid (Depakene), seem to
cause neural tube defects when taken
during pregnancy, possibly because they
interfere with the body's ability to use
folate and folic acid.
Diabetes:
Women with diabetes who don't control
their blood sugar well have a higher risk
of having a baby with spina bifida.
28. Cont…
Obesity:
Pre-pregnancy obesity is associated with an
increased risk of neural tube birth defects,
including spina bifida.
Increased body temperature:
Some evidence suggests that increased body
temperature (hyperthermia) in the early
weeks of pregnancy may increase the risk of
spina bifida.
29. PATHOPHYSIOLOHY
Spina bifida occurs at the end of the first
month of pregnancy when the two sides of
the embryo's spine fail to join together,
leaving an open area.
In some cases, the spinal cord or other
membranes may push through this
opening in the back.
30. DIAGNOSIS
Three tests can check for spina bifida
and other birth defects while the baby
is still in the womb:
Blood test:
A sample of the mother’s blood is tested
to see if it has a certain protein the baby
makes called AFP.
If the level of AFP is very high, it could
mean the baby has spina bifida or another
neural tube defect.
31. Ultrasound:
High-frequency sound waves bounce off
tissues in your body to make black-and-
white pictures of the baby on a
computer monitor.
If your baby has spina bifida, you may
see an open spine or a sac poking out of
the spine.
32. Amniocentesis:
If the blood test shows a high level of AFP but
the ultrasound looks normal, your doctor may
recommend amniocentesis. This is when your
doctor uses a needle to take a small amount of
fluid from the amniotic sac around the baby.
If there’s a high level of AFP in that fluid, that
means the skin around the baby's sac is missing
and AFP has leaked into the amniotic sac.
33. CLINICAL TRIALS
Explore Mayo Clinic studies testing
new treatments, interventions and
tests as a means to prevent,
detect, treat or manage this
disease.
34. IMMEDIATE CARE
Place the child in prone position.
Cover the affected area with sterile
gauze piece dipped in normal
saline.
Maintain hydration.
Monitor for associated defects.
35. TREATMENTS
Spina bifida treatment depends on
the severity of the condition.
Spina bifida occulta often doesn't
require treatment at all, but other
types of spina bifida do.
1. Surgery before birth:
Nerve function in babies with spina
bifida can worsen after birth if it's
not treated. Prenatal surgery for
spina bifida (fetal surgery) takes
place before the 26th week of
pregnancy.
36. Cont…
Surgeons expose a pregnant mother's
uterus surgically, open the uterus
and repair the baby's spinal cord.
Research suggests that children with
spina bifida who had fetal surgery
may have reduced disability and be
less likely to need crutches or other
walking devices. In addition, fetal
surgery may reduce the risk of
hydrocephalus.
37. Cont…
Ask your doctor whether this procedure
may be appropriate for you. Discuss the
risks, such as possible premature delivery
and other complications, and potential
benefits for you and your baby.
38. Cont…
2. Cesarean birth :
Many babies with
myelomeningocele tend to
be in a feet-first (breech)
position. If your baby is in
this position or if your
doctor has detected a large
cyst or sac, cesarean birth
may be a safer way to
deliver your baby.
39. Cont…
3. Surgery after birth:
Meningocele involves surgery to put
the meninges back in place and close
the opening in the vertebrae.
Because the spinal cord develops
normally in babies with meningocele,
these membranes often can be removed
by surgery with little or no damage to
nerve pathways.
40. Cont…
During the procedure, a
neurosurgeon places the spinal
cord and exposed tissue inside
the baby's body and covers
them with muscle and skin.
Sometimes a shunt to control
hydrocephalus in the baby's
brain is placed during the
operation on the spinal cord.
41. Cont…
4. Treatment for complications:
In babies with myelomeningocele,
irreparable nerve damage has likely already
occurred and ongoing care from a
multispecialty team of surgeons, physicians
and therapists is usually needed.
Babies with myelomeningocele may need
more surgery for a variety of complications.
42. LIFE LONG TREATMENT
Catheters
Braces.
High fiber diet.
Antibiotics may be used to treat or
prevent infections such as meningitis
or urinary tract infections.
43. SOCIAL IMPACT
Compared to typically developing
children, youths with spina bifida may
have fewer friends and spend less time
with peers.
Most children that are treated early
will have normal IQ and be able to
attend public schools.
44. Cont…
Mobility is the biggest concern for many
patients with spina bifida - lack of
mobility can lead to obesity and
scoliosis
With proper treatment, individuals will
live well into adulthood
45. CONCLUSIONS
Patient neurological deficit improve in
50% & stabilize in another 40%
following surgery
Is a multidisciplinary problem
Planning necessary
Asymptomatic cases should be operated
Surgery for paraplegic patient
controversial (We operate after full
discussion with family)
46. REFERENCE
Appelmann, L. (2002). Living with spina bifida.
Victoria, B.C.: Trafford.
Llewellyn, G. and Green, L. (1990). Living
with spina bifida. Lidcombe, N.S.W.:
Cumberland College of Health Sciences, The
University of Sydney.
Ozek, M. (2014). Spina bifida. [Place of
publication not identified]: Springer.
Google Search Engine.
47. Cont…
Mark R Foster, P. (2019). Spina Bifida
Treatment, Causes, Symptoms & Life
Expectancy. [online] eMedicineHealth. Available
at:
https://www.emedicinehealth.com/spina_bifid
a/article_em.htm [Accessed 10 Mar. 2019].
Mayo Clinic. (1998). Spina bifida - Symptoms
and causes. [online] Available at:
https://www.mayoclinic.org/diseases-
conditions/spina-bifida/symptomscauses/syc-
20377860 [Accessed 10 Mar. 2019].