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CONGENITAL ABNORMALITIES
IN NEWBORNS & INFANTS
By; Asaba Marion
MMW, BScn& PGDME
Sch. of Nursing & Midwifery Bugema Univ.
Learning objectives
Define congenital abnormality
Mention the common types of congenital
abnormalities
Check each newborn baby to be sure that there is no
congenital anomaly
Provide appropriate care for babies with congenital
abnormalities
Definition
• Congenital abnormalities are also known as birth defects,
congenital anomalies or congenital malformations.
• Congenital anomalies can be defined as structural or
functional anomalies (for example, metabolic disorders) that
occur during intrauterine life and can be identified
prenatally, at birth, or sometimes may only be detected later
in infancy, such as hearing defects.
• In simple terms, congenital refers to the existence at or
before birth.
Food for thought.
•What is the cause of death in neonates with
congenital life during the first one month
compared to the rest of the months?
Disease Burden
• An estimated 303 000 newborns die within 4 weeks of birth
every year, worldwide, due to congenital anomalies.
• Causes of 2.68 million deaths during the neonatal period in
2015, worldwide
• Congenital anomalies can contribute to long-term disability,
which may have significant impacts on individuals, families,
health-care systems, and societies.
Causes /predisposing factors
• Although approximately 50% of all congenital anomalies cannot be linked
to a specific cause
• Genetic factors
• Socioeconomic and demographic factors
• Environmental factors
• Infections
• Maternal nutrition status
• Etc.
Some common congenital abnormalities
•Cleft lip & palate
•Club foot
•Spinal bifida
•Hydrocephaly
• Cryptorchidism
• Imperforated anus
• Umbilical hernia
• Pyloric stenosis
• Phimosis & paraphimosis
• etc
Cleft lip and cleft palate
• Cleft lip and cleft palate are problems of the mouth and lip.
• They affect about 1 in every 1,000 births.
• Cleft lip and cleft palate develop early in pregnancy when the
sides of the lip and the roof of the mouth do not fuse together as
they should.
• Cleft lip and cleft palate are caused by several genes inherited
from both parents.
• They are also caused by environmental things that scientists don’t
yet fully understand
Normal
Cleft palate
• Cleft palate happens when
the roof of the mouth does
not completely close.
• This leaves an opening that
can extend into the nasal
cavity.
• Cleft palate is not as
noticeable as cleft lip
because it is inside the
mouth.
Cleft lip
• This happens when the lip doesn’t
completely form in the womb
(uterus).
• How serious the cleft lip is can vary
greatly.
• The child may have a mild form,
such as a notching of the lip.
• Or the child could have a severe
form, with a large opening from
the lip up through the nose.
Concerns
•To parent, its stressful to adjust to the obvious
problem of the face, because it is so easily
noticed.
•Feeding problems
•Speech & language development difficulties
•Ear infections
•Dental infections
Treatment
• Treatment for cleft lip and cleft palate includes
surgery.
• A cleft lip can be repaired within the first several
months of life.
• Cleft palate repairs are usually done when the baby
is 9 to 18 months old, but before the age of 2.
Club foot( talipes)
• Club foot is a foot which has been distorted out of shape or
position in utero and cannot be moved to uncorrected
position.
• The foot appears to be in form of a club.
• Types of club foot
• 1. talipes equinovarus
• 2. talipes calcaneovalgal
• Both types are usually bilateral.
•In talipes equinovarus,
the foot is fixed in
plantar fixation
&deviates medially, i.e
the heel is elevated.
•The child walks on toes
• In talipes calneovagal as the foot
is dorsiflexed & deviates lateral,
i.e the heel is turned outward, &
anterior part of the food s
elevated on the outer border.
• The child walks on the outwardly
turned heel& the inner border of
the foot.
Treatment & nurses responsibilities
• Treatment must be started as soon as possible.
• Delay makes correction more difficult, since the bones &
muscles of the legs develop abnormally & the tendons will
be shortened.
• In infancy, application of the cast to hold the foot in correct
position maybe used.
• The nurse may be responsible 4 immobilization& holding the
child during cast application
• If the measure fails to correct, surgery on the tendons &
bones may be done in early childhood, & the legs and foot
placed in a cast
• Preparation for pre and post operation procedures

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CONGENITAL ABNOR NEWBORNS & INFANTS.pptx

  • 1. CONGENITAL ABNORMALITIES IN NEWBORNS & INFANTS By; Asaba Marion MMW, BScn& PGDME Sch. of Nursing & Midwifery Bugema Univ.
  • 2. Learning objectives Define congenital abnormality Mention the common types of congenital abnormalities Check each newborn baby to be sure that there is no congenital anomaly Provide appropriate care for babies with congenital abnormalities
  • 3. Definition • Congenital abnormalities are also known as birth defects, congenital anomalies or congenital malformations. • Congenital anomalies can be defined as structural or functional anomalies (for example, metabolic disorders) that occur during intrauterine life and can be identified prenatally, at birth, or sometimes may only be detected later in infancy, such as hearing defects. • In simple terms, congenital refers to the existence at or before birth.
  • 4. Food for thought. •What is the cause of death in neonates with congenital life during the first one month compared to the rest of the months?
  • 5. Disease Burden • An estimated 303 000 newborns die within 4 weeks of birth every year, worldwide, due to congenital anomalies. • Causes of 2.68 million deaths during the neonatal period in 2015, worldwide • Congenital anomalies can contribute to long-term disability, which may have significant impacts on individuals, families, health-care systems, and societies.
  • 6. Causes /predisposing factors • Although approximately 50% of all congenital anomalies cannot be linked to a specific cause • Genetic factors • Socioeconomic and demographic factors • Environmental factors • Infections • Maternal nutrition status • Etc.
  • 7. Some common congenital abnormalities •Cleft lip & palate •Club foot •Spinal bifida •Hydrocephaly • Cryptorchidism • Imperforated anus • Umbilical hernia • Pyloric stenosis • Phimosis & paraphimosis • etc
  • 8. Cleft lip and cleft palate • Cleft lip and cleft palate are problems of the mouth and lip. • They affect about 1 in every 1,000 births. • Cleft lip and cleft palate develop early in pregnancy when the sides of the lip and the roof of the mouth do not fuse together as they should. • Cleft lip and cleft palate are caused by several genes inherited from both parents. • They are also caused by environmental things that scientists don’t yet fully understand
  • 10. Cleft palate • Cleft palate happens when the roof of the mouth does not completely close. • This leaves an opening that can extend into the nasal cavity. • Cleft palate is not as noticeable as cleft lip because it is inside the mouth.
  • 11. Cleft lip • This happens when the lip doesn’t completely form in the womb (uterus). • How serious the cleft lip is can vary greatly. • The child may have a mild form, such as a notching of the lip. • Or the child could have a severe form, with a large opening from the lip up through the nose.
  • 12. Concerns •To parent, its stressful to adjust to the obvious problem of the face, because it is so easily noticed. •Feeding problems •Speech & language development difficulties •Ear infections •Dental infections
  • 13. Treatment • Treatment for cleft lip and cleft palate includes surgery. • A cleft lip can be repaired within the first several months of life. • Cleft palate repairs are usually done when the baby is 9 to 18 months old, but before the age of 2.
  • 14. Club foot( talipes) • Club foot is a foot which has been distorted out of shape or position in utero and cannot be moved to uncorrected position. • The foot appears to be in form of a club. • Types of club foot • 1. talipes equinovarus • 2. talipes calcaneovalgal • Both types are usually bilateral.
  • 15. •In talipes equinovarus, the foot is fixed in plantar fixation &deviates medially, i.e the heel is elevated. •The child walks on toes
  • 16. • In talipes calneovagal as the foot is dorsiflexed & deviates lateral, i.e the heel is turned outward, & anterior part of the food s elevated on the outer border. • The child walks on the outwardly turned heel& the inner border of the foot.
  • 17. Treatment & nurses responsibilities • Treatment must be started as soon as possible. • Delay makes correction more difficult, since the bones & muscles of the legs develop abnormally & the tendons will be shortened. • In infancy, application of the cast to hold the foot in correct position maybe used. • The nurse may be responsible 4 immobilization& holding the child during cast application
  • 18. • If the measure fails to correct, surgery on the tendons & bones may be done in early childhood, & the legs and foot placed in a cast • Preparation for pre and post operation procedures