I prepared this presentation during the first year of my MDS. This will give you a basic idea and necessary information about the pulp of the teeth and its histology. Hope you guys find it useful.
Central face begins to develop by 4th week, when olfactory placodes appear on both sides of the frontonasal process.
Gradually both placodes develop to form the median and lateral nasal process.
Upper lip is formed by 6th week by fusion of two median nasal processes in midline and the maxilllary process of the 1st branchial arch.
PRE-NATAL GROWTH AND DEVELOPMENT OF PALATEFormation of primary and secondary palate
Elevation of palatal shelves
Fusion of palatal shelves
I prepared this presentation during the first year of my MDS. This will give you a basic idea and necessary information about the pulp of the teeth and its histology. Hope you guys find it useful.
Central face begins to develop by 4th week, when olfactory placodes appear on both sides of the frontonasal process.
Gradually both placodes develop to form the median and lateral nasal process.
Upper lip is formed by 6th week by fusion of two median nasal processes in midline and the maxilllary process of the 1st branchial arch.
PRE-NATAL GROWTH AND DEVELOPMENT OF PALATEFormation of primary and secondary palate
Elevation of palatal shelves
Fusion of palatal shelves
Neural crest cells / dental implant courses by Indian dental academy Indian dental academy
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The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
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BE UPDATE TO IT,, AS IT IS 3 years back from 2017
Kindly mail me if you feel, needy of this presentation
you can find my mail id @ slide share,,, if not mail me @
sukesh3567@gmail.com.
Good luck
THEORIES OF ERUPTION
ERUPTION SEQUENCE
PHYSIOLOGY OF TOOTH ERUPTION
CELLULAR BASIS
MOLECULAR BASIS
PRODUCTION OF OSTEOCLAST
ANOMOLIES OF TOOTH ERUPTION
Neural crest cells / dental implant courses by Indian dental academy Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
BE UPDATE TO IT,, AS IT IS 3 years back from 2017
Kindly mail me if you feel, needy of this presentation
you can find my mail id @ slide share,,, if not mail me @
sukesh3567@gmail.com.
Good luck
THEORIES OF ERUPTION
ERUPTION SEQUENCE
PHYSIOLOGY OF TOOTH ERUPTION
CELLULAR BASIS
MOLECULAR BASIS
PRODUCTION OF OSTEOCLAST
ANOMOLIES OF TOOTH ERUPTION
DEVELOPMENT OF FACE/ Development of face, palate and jawDishikaBhagwani27
• Introduction, General embryology○ Fertilization ○ Formation of germ layers ○ Development of face – •Pharyngeal arches, pouch & clefts ○ Development of nose. development of maxilla & mandible, development of eyes,development of lips & checks Development of head • Development of skull • Development of face.....
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This is a slide for complete development in chick ,as chick is a vertebrate so with the help of the development in a chick we can we can understand development in vertebrates .
This topic explains the whole process of growth and development in animal the processes include
Fertilization and incubation
Cleavage
Morula
Blastula
Gastrulation
Notochord And Mesoderm Formation
Neurulation
Embryonic Gastrulation by Maryam Borhani-Haghighiborhanihm
Gastrulation is a phase in the embryonic development during which the single-layered blastula is reorganized into a trilaminar ("three-layered") structure known as the gastrula.
Similar to General embryology growth & development of mandible (20)
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
2. CONTENTS :
INTRODUCTION - A general aspect
GROWTH & DEVELOPMENT
FERTILIZATION
CLEAVAGE
FORMATION OF GERM LAYERS,
NOTOCHORD, NEURAL TUBE & YOLK SAC
THE PHARENGEAL ARCHES
FATE OF GERM LAYERS
PRE-NATAL DEVELOPMENT OF MANDIBLE
POST-NATAL DEVELOPMENT OF
MANDIBLE
APPLIED ASPECTS
2
3. INTRODUCTION – GENERAL
ASPECT
The study of formation & development of
embryo from the moment of its inception up to
the time when it is born as an infant is called
EMBRYOLOGY.
3
4. There are 2 types cell division
MITOSIS MEIOSIS
MITOSIS : when the cell divides so that no.of
chromosomes and genetic configuration remains the
same. Daughter cells have diploid no.of
chromosomes (46).
MEIOSIS : The no.of chromosomes is halved and
the genetic information is not absolutely identical.
Gametes resulting due to meiosis have haploid no.of
chromosomes (23).
4
5. GROWTH & DEVELOPMENT
Growth is an increase in size.
Development is progress towards maturity.
- TODD
5
6. PERIODS OF PRE-NATAL
DEVELOPMENT
PROLIFERATIVE PERIOD : Implantation and
enlargement of blastocyst occurs within 2 weeks
of development called proliferative period.
EMBRYONIC PERIOD : This ranges from 3-8
weeks and is the differentiation of the three basic
tissue types and their specialization into organs
and organ systems.
FETAL PERIOD : This is the period of growth.
6
7. FERTILIZATION
The process of fusion of the male gamete (
sperm/spermatozoa ) with the female gamete (
ovum/oocyte ) is called FERTILIZATION.
Fertilization takes place in the ampulla of the
uterine tube.
This fusion results in the formation of ZYGOTE.
As a result of fertilization
> the diploid no.of chromosomes is restored
> determination of sex takes place
> fertilized ovum begins to undergo division
7
10. CLEAVAGE
The fertilized ovum undergoes a series of mitotic
divisions leading to
3-cell stage , 4-cell stage , 5-cell stage etc.
This process of subdivision is called CLEAVAGE.
As this process continues the 16-cell stage is
called a MORULA.
A cut section reveals INNER CELL MASS that is
surrounded by a layer of outer cells.
The outer cells give rise to TROPHOBLAST & the
inner cell mass gives rise to EMBRYOBLAST.
10
11. Fluid passes from into the morula from the
uterine cavity and separates the ICM and the
trophoblast hence the morula acquires the
shape of a cyst.
Trophoblast cells become flat and ICM
attaches to one side of the trophoblast. This
stage is now called the BLASTOCYST & the
cavity is called the BLASTOCOELE.
The side where ICM is attached is called
EMBRYONIC or ANIMAL pole and the
opposite side is called the ABEMBRYONIC
pole.
11
14. FORMATION OF GERM
LAYERS
There is formation of a 3 layered disc as the
blastocyst develops called EMBRYONIC
DISC.
The 3 germ layers making up this disc are
Endoderm
Ectoderm
Mesoderm
14
15. Some cells of the ICM differentiate into flat cells that
line the surface hence forming the 1st germ layer, i.e
the endoderm
Remaining ICM cells become columnar forming the
2nd germ layer , i.e the ectoderm.
A space appears between ectoderm & trophoblast
called AMNIOTIC CAVITY filled with AMNIOTIC
FLUID .
The flattened cells spread & line the blastocystic
cavity . This lining is called HEUSER’S MEMBRANE ,
resulting cavity is called PRIMARY YOLK SAC.
The cells of the trophoblast give rise to
EXTRAEMBRYONIC MESODERM . These lie
between trophoblast & flat endodermal cells .
15
18. Small cavities appear in the EEM which join
together to form one large cavity called
EXTRAEMBRYONIC COELOM, thus resulting
in splitting of EEM.
The part lining the inside of the trophhoblast
and outside amniotic cavity is called
PARIETAL MESODERM
(somatopleuric EEM or Chorionic plate)
The part lining the outside of the yolk sac is
called the VISCERAL MESODERM.
The developing embryo is now suspended in
the EEC and is attached to the wall of the
blastocyst by the unsplit part of EEM.
This forms the CONNECTING STALK.
18
20. Two important structures are formed at this
stage
CHORION: the trophoblast & underlying
somatopleuric mesoderm form chorion
AMNION: the cells forming the wall of the
amniotic cavity form the amnion.
Due to EEM & EEC the yolk sac becomes
smaller and is now called the SECONDARY
YOLK SAC.
The lining cells now become cubical.
20
22. At one circular area near the margin of the disc,
the cubical cells of the endoderm become
columnar forming the PROCHORDAL PLATE.
Some ectodermal cells near the tail end proliferate
& form an elevation that bulges into amniotic
cavity . This elevation is PRIMITIVE STREAK.
The cells that proliferate pass sideways, pushing
between the ectoderm & endoderm forming the
INTRAEMBRYONIC MESODERM.
This process of formation of primitive streak & IEM
is called GASTRULATION.
22
27. Cranial end of the primitive streak enlarges to form the
PRIMITIVE KNOT.
A depression appears in this structure called
BLASTOPORE, which later converts into NOTOCHORDAL
CANAL.
Cells of the primitive knot multiply & pass cranially to form a
rod like structure reaching up to the prochordal plate. This
is the NOTOCHORDAL PROCESS.
The notochordal process undergoes changes to convert it
into a canal and then a plate and finally into a rod like
structure called NOTOCHORD.
Wide strip of ectoderm overlying the notochord becomes
thickened and forms the NEURAL PLATE which forms the
brain and spinal cord.
Process of formation of the neural tube is called
NEURALISATION.
27
29. The IEM shows 3 subdivisions
PARA-AXIAL mesoderm: mesoderm next to midline which
undergoes segmentation to form SOMITES.
LATERAL PLATE mesoderm: mesoderm in the lateral
part of the embryonic mesoderm.
Cavity called INTRA EMBRYONIC COELOM appears in
the lateral plate mesoderm and splits it into
SOMATOPLEURIC & SPLANCHOPLEURIC layer.
INTERMEDIATE mesoderm: layer betwen para-axial and
lateral plate mesoderm.
The embryonic disc undergoes foldings at the cranial and
caudal ends called HEAD & TAIL FOLDINGS.
29
31. Lateral folds also appear and the endoderm is
converted into a gut that is divisible into
foregut, midgut & hindgut.
After formation of the head fold, the gut is
closed cranially by the prochordal plate, which
is now called the BUCCOPHARENGEAL
MEMBRANE.
Caudally the gut is closed by the CLOACAL
MEMBRANE.
31
36. THE PHARENGEAL ARCHES
The foregut is bound ventrally by the pericardium,
dorsally by the developing brain, cranially it is at first
separated from the stomatodeum by the
buccopharengeal membrane.
When this membrane breaks down, the foregut opens to
the exterior through the stomatodeum.
Rod like thickenings of the mesoderm present in cranial
most part of the foregut are called PHARENGEAL
ARCHES.
The endodermal wall of foregut is separated from the
surface ectoderm by a layer of mesoderm.
Soon the mesoderm arranges in the form of 6 bars that
run dorsoventrally in the side wall of the foregut.
36
37. Each of these bars grow ventrally in the floor of the
developing pharnyx and fuses with the corresponding
bar of the opposite side to form a PHARENGEAL
ARCH.
In the interval between two arches, the endoderm
(lining the pharynx) is pushed outwards to form a
series of pouches called PHARENGEAL ARCHES.
Opposite each pouch the surface ectoderm dips
inwards forming an ECTODERMAL CLEFT.
There are 6 branchial arches.
1st BA- Mandibular Arch
2nd BA-Hyoid Arch
3rd 4th 5th 6th BA’s have no special names and the 5th BA
soon dissapears after its formation.
37
38. Structures formed in mesoderm of each arch :
Skeletal Element – this is cartilaginous in the
beginning . It may develop into bone , may disappear
or may remain cartilaginous.
Straited Muscle- This is supplied by the nerve of the
arch. It may or may not retain the attachment to the
skeletal elements or may divide to form a no.of
distinct muscles.
Arterial Arch-ventral to foregut is the VENTRAL
AORTA and dorsally there is DORSAL AORTA. A
series of arterial arches/aortic arches connect these
two aorta. One such arterial arch lies in each
pharengeal arch.
38
45. PRE-NATAL DEVELOPMENT OF
MANDIBLE
Mandibular arch gives off a bud from its dorsal end
called MAXILLARY PROCESS.
It grows ventro-medially cranial to main part of the arch
which is called the MANDIBULAR PROCESS.
Mandibular process of each side grow towards each
other and fuse in midline to give rise to mandible.
First structure to develop in lower jaw :
Mandibular division of Trigeminal nerve.
Neurotrophic factor produced by nerve induces
osteogenesis.
45
48. Primary cartilage of first pharyngeal arch is
Meckel’s cartilage & it helps in formation of lower
jaw.
Meckel’s cartilage first appears at 6th week IUL.
It is a solid hyaline cartilaginous rod surrounded by
fibrocellular capsule.
Ossification starts at the division of mental and
incisive branch of inferior alveolar nerve lateral to
meckel’s cartilage around 6th week IUL.
48
49. From center of ossification bone formation
spreads:
Anteriorly - midline
Posteriorly - where mandibular nerve divides
into lingual and inferior alveolar branch.
Bone formation spreads rapidly and
surrounds the inferior alveolar nerve to form
mandibular canal.
Intramembranous ossification spreads in
anterior and posterior direction forms the
Body & Ramus of the mandible.
49
51. Anteriorly bone extends towards midline and comes in
approximation with similar bone forming on opposite
side.
These two bones remain separated by fibrous tissue
mental symphysis untill shortly after birth.
Continued bone formation increases size of mandible
with development of alveolar process to surround the
developing tooth germ.
Ossification spreads posteriorly to form ramus of
mandible, turning away from meckel’s cartilage.
This point of divergence is marked by lingula in adult
mandible.
51
53. FATE OF THE MECKEL’S CARTILAGE :
Lacks enzyme phosphatase found in ossifying
cartilage thus precluding its ossification.
Greater part of meckel’s cartilage degenerates
without contributing formation of mandible by 24th
week.
Most posterior extremity forms incus and malleus of
inner ear.
Fibrocellular capsule persists as sphenomandibular
ligament.
Small part of its ventral end forms accesory
endochondral ossicles.
Gets incorporated in the chin region of the mandible.
53
54. SECONDARY CARTILAGES:
Further growth until birth is influenced by appearance of
secondary cartilage .
Between 10th and 14th week three secondary cartilages
develop:
Condylar cartilage – largest and appears beneath the
fibrous articular layer of future condyle.
Coronoid cartilage - seen associated with coronoid
process.
Symphyseal cartilage – in the mandibular symphysis
region.
Mandible develops largely by intramembranous
ossification and by endochondral ossification in
Condylar process
Coronoid process
Mental region
54
55. CONDYLAR PROCESS
Develops from condylar cartilage & appears as
separate area of mesenchymal condensation along
developing mandible around 8th week.
This area develops in cone-shaped cartilage around
10th week.
By the 14th week first evidence of endochondral bone
formation appears in condylar region.
Cartilage fuses with mandibular ramus around 4th
month.
Cartilage replaced by bone but upper end persists in
adulthood acting as Growth and Articular cartilage.
55
57. CORONOID PROCESS
Secondary cartilage appears in coronoid
process around 10-14th week.
Cartilage grow as a response of developing
temporalis muscle.
Coronoid cartilage becomes incorporated into
expanding intramembranous bone of ramus
and disappears before birth.
57
58. MENTAL REGION
Throughout intrauterine life left and right
mandible are not fused at midline.
Joined by connective tissue at midline.
On either side of symphysis, symphyseal
cartilage appears between 10th & 14th week
post conception.
Ossifies in the 7th month to form mental
ossicles in fibrous tissue of symphysis.
Mental ossicles fuse with mandibular body at
the end of first year after birth.
58
59. POST-NATAL DEVELOPMENT
OF MANDIBLE
Of the facial bones, the mandible undergoes
the largest amount of growth post-natally and
also exhibits the largest variability in
morphology
The basal bone or the body of mandible
forms one unit, to which is attached the
alveolar process, the coronoid process, the
condylar process, the angular process, the
ramus, the lingual tuberosity and the chin.
59
60. RAMUS & BODY OF MANDIBLE
The ramus moves progressively posterior by a
combination of deposition and resorption
Resorption occurs on the anterior part of the ramus
while bone deposition occurs on the posterior region.
This results in drift of ramus in a posterior direction
Body of the mandible lengthens as the ramus exhibits
bone deposition on the posterior aspect and
resorption on the anterior aspect
60
62. ANGLE OF MANDIBLE
On the lingual side of the angle of the mandible,
resorption takes place on the posterio-inferior aspect
while deposition occurs on the antero-superior aspect
On the buccal side, resorption occurs on the anterio-
superior part while deposition takes place on the
postero-inferior part. This results in flaring of the angle
of the mandible as age advances
62
64. LINGUAL TUBEROSITY
The lingual tuberosity moves posteriorly by
deposition on its posterior facing surface
Lingual tuberosity protrudes noticeably in a lingual
direction and that it lies well towards the midline of
the ramus.
The prominence of the tuberosity is increased by the
presence of a large resorption field just below it.
The resorption field produces a sizeable depression,
called the LINGUAL FOSSA.
64
66. ALVEOLAR PROCESS
As the teeth erupt the alveolar process develops and
increases in height by bone deposition at the margins
The alveolar process adds to the height and
thickness of the body of the mandible
In case of absence of teeth, the alveolar bone fails to
develop and it resorbs in the event of tooth extraction
66
67. THE CONDYLE
The role of condyle in the growth of mandible has
remained a controversy. There are 2 schools of
thought regarding the role of the condyle:
It was earlier believed that growth occurs at the
surface of condylar cartilage by means of bone
deposition.
It is now believed that the growth of soft tissues
including the muscles and connective tissues carries
the mandible forward & away from the cranial base
(carry away phenomenon).
67
69. CORONOID PROCESS
The growth of the coronoid process follows the
enlarging “V” principle
Viewing the longitudinal section of the coronoid
process from the posterior aspect, deposition occurs
on the lingual surfaces of the left and right coronoid
process
Viewing it from the occlusal aspect, the deposition on
the lingual of the coronoid process brings about a
posterior growth movement in the “V” pattern.
69
71. THE CHIN
The chin is associated with a generalised cortical
recession in the flattened regions positioned between
the canine teeth.
The process involves a mechanism of endosteal
cortical growth.
Prominence of mental protuberance is accentuated
by bone resorption that occurs in the alveolar region
above it, creating a concavity.
71
73. Micrognathia - Small jaw size
Macrognathia - Big jaw size
Agnathia - Total failure of development
Microstomia - Excess fusion of the maxillary and
mandibular processes may result in microstomia.
Macrostomia - Inadequate fusion of the maxillary
and mandibular processes with each other may lead
to an abnormally wide mouth. Lack of fusion may be
unilateral leading to lateral facial cleft.
73
75. Hemifacial microsomia –
Also called goldenhar syndrome
Due to lack of mesenchymal tissue or neural crest
cells resulting in underdeveloped mandible
75
76. Midline mandibular cleft
Persistance of furrow between 2 mandibular
prominences
76
77. Mandibular Dysostosis –
also called Treacher-collins syndrome
Due to disturbance in origin, migration &
interaction of neural crest cells.
Hypoplasia of mandible
77
78. Pierre-Robin Syndrome -
Mandible is underdeveloped
Small body
Posteriorly placed condyle
Cleft palate
78
79. Bifid condyle –
Rare
Most of them have a medial and lateral head
that is divided by an antero posterior groove.
Some condyles may be divided into an anterior
and posterior head
Cause is uncertain
79
80. Condylar hyperplasia –
Excessive growth of one of the condyles.
Cause is unknown, but local circulating
problems, endocrine disturbances, and trauma
have been suggested as possible etiologic
factors.
80
81. REFERENCES
HUMAN EMBRYOLOGY - I.B.SINGH
ESSENTIALS OF ORAL HISTOLOGY & EMBRYOLOGY
- AVERY
ESSENTIALS OF HUMAN EMBRYOLOGY -
B.S.PANDE
TEXTBOOK OF ORTHODONTICS - BALAJI
TEXTBOOK OF ORTHODONTICS -
GURKHEERAT SINGH
Enlow DH, Harris DB – A study of the postnatal growth
of the human mandible, - Am J Orthod,1964;50:250-64
Sicher H - The growth of the mandible - Am J Orthod,
1947;33:30-35
81
46 chromosomes or 23 pairs.
22 identical and 1 pair is the sex choromosomes, i.e 44 autosomes and 2 sex chromosomes
Gametes- cells that carry out the function of reproduction.
Process of formation of gametes- spermatogenesis , oogenesis
16 – cell stage looks like a mulberry.
It is still surrounded by the zona pellucida.
Trophoblast cells provides nutrition to the embryo.
It is called an embryoblast as it gives rise to the embryo proper.
Embryo proper = embryoblast.
Fluid quantity increases and gives the shape of cyst to morula.
Cyst defination-
32 cell stage is called the blastocyst.
The embryo proper is at this stage composed of 2 layers of cells – the upper layers (towards amniotic cavity) is the ectoderm – cells are columnar
The lower layer (towards yolk sac) is the endoderm – cells are cubical
No indication yet of head or tail end of embryonic disc.
This helps us to determine central axis of the embryo - differentiate between the left and right halves and also the future head and tail ends.
Primitive streak later becomes a linear structure lying in the central axis of disc.
IEM=secondary mesoderm.
The IEM spreads through out except in the region of the prochordal plate. It extends cranial to the prochordal plate and it from the 2 sides becomes continuous across the midline. As there is no mesoderm in the region of prochordal plate , the region is thin and it later forms the buccopharengeal membrane.
The ectoderm and endoderm persist as lining memebrane.
The primitive streak eventually elongates and becomes pear shaped.
The stalk becomes comparatively smaller as the embryonic disc enlarges in size so the attachment remains confinied to the region of the tail end of the embryonic disc. Some IEM passes backwards into the connecting stalk and leaves an area where the endoderm and ectoderm are in contact. This is similar to prochordal plate and forms cloacal membrane.
Primitive knot=primitive node=hensens node
Notochordal process=head process
Notochordal canal communicates with the amniotic cavity through the blastopore
Most of the notochord disappears and remenants remain as the nucleus pulposus of each intervertebral dsic.
The neural tube arises distal to the notochord by the infolding of the neural folds. These crests give rise to neural crest cells that behave like mesoderm and are hence called the ectomesenchyme.
SOMATOPLEURIC layer – in contact with the ectoderm
SPLANCHOPLEURIC layer- in contact with the endoderm