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UMBILICAL
CORDDr. Sherif Fahmy
Morphology of Umbilical Cord
It is the connection between placenta and
fetus.
• Length: 50 – 60 cm
• Diameter: 2 cm.
• Shape: Tortous, showing false notes.
• Contents: 2 umbilical arteries, one umbilical vein
embedded in wharton’s jelly and surrounded by
amniotic membrane.
• Attachments: It is attached to fetal surface of placenta
near its center, the other attachment is to ventral
aspect of fetal abdominal wall.
• Functions:
– It contains umbilical vessels that connect the fetus to the
placenta.
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Development of the Cord
• Primitive umbilical ring:
- Expansion of amniotic cavity, leads to folding with
ventral shifting of amnio-ectodermal junction and
formation of primitive umbilical ring
- Contents:
-Connecting stalk containing allantois and umbilical
vessels.
-Vitelline duct and vitelline vessels.
-Connection between intraembryonic and extra-
embryonic coelom.
Dr. Sherif Fahmy
Primitive umbilical cord:
- Expansion of amniotic cavity, leads to
elongation of umbilical cord.
Contents:
1- Yolk sac and vitelline duct.
2- Connecting stalk with remnant of allantois.
3- Intestinal loop in its proximal part.
4- Umbilical and vitelline vessels.
Dr. Sherif Fahmy
Definitive umbilical cord:
- Return of intestinal loop to abdominal cavity at
3rd
month.
-Obliteration of vitelline duct, allantois, extra-
embryonic part of vitelline vessels.
-Degeneration of one umbilical vein with
persistence of other vein and 2 umbilical
arteries.
-Transformation of mesoderm of connecting
stalk into wharton’s jelly.
Development
Embryonic disc with removed
ectoderm
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
• Abnormalities of Umbilical Cord
• 1- Short cord: leads to premature separation
of placenta.
• 2- Long cord: It may encircle neck of fetus and
may form true knots.
• 3- Congenital umbilical hernia
(omphalocele): the cord contains coils of
intestine.
• 4- Presence of one umbilical artery.
• 5- Abnormal attachment of the cord:
–Marginal attachment (battledore)
–Through membranes (velamentous).
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Dr. Sherif Fahmy
Twins
Dr. Sherif Fahmy
Types of TWINS
Dizygotic (Fraternal) twins:
- It is the commonest type as it represent 2/3 of
twins and 7 – 11 / 1000 births.
- Fertilization of 2 separate ova.
- Each embryo has its own placenta, chorion
and amniotic cavity.
- Twins are non-identical and may of same sex
or different.
Dr. Sherif Fahmy
Monozygotic (Identical) twins:
Developed from division of a fertilized ovum. Twins of this type are
identical and of same sex. Its incidence is 0.3 – 0.4 %
Division may occure at 3 different stages:
1- At morula stage: Twins has separate amnion,
chorion and placentae (as in dizygotic).
2- At blastocyst stage: due to division of inner cell
mass. Twins has separate amniotic cavity but single
chorion and placenta.
3- At embryonic disc: Midline division of the embryonic
disc. Twins has common amniotic cavity, common
chorion and common placenta .
Dr. Sherif Fahmy
Morula
stage
EmbryonicDisc StageEarly
blastcyste
Dr. Sherif Fahmy
SIAMESE (CONJOINED) TWINS
• Fused monozygotic twins that occurs
due to incomplete separation of
emberyonic disc. They could be
either:
Craniopagus: Fusion between 2 heads.
Thoracopagus: Fusion at thoracic region.
Pygopagus: Fusion at the pelvic region.
Dr. Sherif Fahmy
Conjoined Twines
Dr. Sherif Fahmy
Birth DefectsDr. Sherif Fahmy
Dr. Sherif Fahmy
1- Enviromental Factors
• Infectious Agents: Viruses, Bacteria and
parasites.
• Radiations: X-ray, Gamma and atomic
radiation.
• Drugs & chemicals: e.g. antiepileptic drugs,
vit. A, Alcohol
• Maternal diabetes:
Dr. Sherif Fahmy
Chromosomal
1- Numerical Chromosomal Anomalies
A-Autosomal:
• A- Triosomy 21 (Down or Mongolism).
• Each cell contains 47 chomosomes (45 + XX or
XY).
• B- Triosomy 13, 15, 17 & 18.
Dr. Sherif Fahmy
B- Sex Numerical Chromosomal Anomalies
• 1- Klinefelter syndrome: (44 + XXy)
Due to non-disjunction of X chromosome. Male
case suffers from infertility and gynecomastia.
• 2- Turner syndrome: (44 + X0)
Due to non-disjunction of X chromosome.
Female case suffers from gonadal dysgenesis,
short staure and neck skin fold
Dr. Sherif Fahmy
2- Structural Chromosomal Anomaly
• A- Cri-du-Chat Syndrome.
Due to partial deletion of short arm of
chromosome 5 (cat-like cry, microcephaly and
mental retardation).
• B- Angelman Syndrome.
Partial deletion of long arm of chromosome 15
(mental retardation, poor motor development
and prolonged period of laughter.
Dr. Sherif Fahmy
Down Syndrome
Dr. Sherif Fahmy
Cri du Chat Syndrome
Turner Syndrome
Achondroplasia
A Child of Alcoholic Mother
A Child of A Mother Treated by
Antiepileptic drug
A Child of A Mother Treated with
Antithyroid drug
A Child of A mother Exposed to
Rubella Infection
External Appearance of the Embryo
(4th
– 8th
week)
At the embryonic period (4th
– 8th
week),
human shape becomes easily identified.
-Head, body and limb buds are easily
identified.
-Eyes, nose and ears are seen.
C-R length in mms Age of embryo in weeks
5 – 8 5
10 – 14 6
17 – 22 7
28 – 30 8
Fetal Period
C-R length in cm Age of embryo in months
5 – 8 cm 3rd
month
18 cm 5th
month
36 cm Full term fetus at birth
Relative size of head to body:
-At the beginning of the 3rd
month, the head is ½
the CR length.
-At the beginning of the 5th
month, the head is 1/3
the CH length.
-At birth, the head is ¼ of CH length.
Weight growth:
-At the end of 5th
month, the weight is ½ kg.
-At the 7th
month, the weight is 1.75 kg.
-At full term, the weight is 3.5 kg.
Changes in external features:
-Face becomes human looking.
-Limbs become longer.
-External genitalia are differentiated at 12th
week.
-Lanugo hair covers the fetus since the 4th
month.
-The skin is wrinkled till the end of 6th
month.
-Testes descend to scrotum just before birth.
-Skin is covered by fatty substance called vernix
caesosa.
Fetal movement:
It is clearly recognized since the 5th
month.
The End &
Beginning
With my best wishes
Dr. Sherif Fahmy

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Umbilical Cord (General Embryology)

  • 2. Morphology of Umbilical Cord It is the connection between placenta and fetus. • Length: 50 – 60 cm • Diameter: 2 cm. • Shape: Tortous, showing false notes. • Contents: 2 umbilical arteries, one umbilical vein embedded in wharton’s jelly and surrounded by amniotic membrane. • Attachments: It is attached to fetal surface of placenta near its center, the other attachment is to ventral aspect of fetal abdominal wall. • Functions: – It contains umbilical vessels that connect the fetus to the placenta. Dr. Sherif Fahmy
  • 5. Development of the Cord • Primitive umbilical ring: - Expansion of amniotic cavity, leads to folding with ventral shifting of amnio-ectodermal junction and formation of primitive umbilical ring - Contents: -Connecting stalk containing allantois and umbilical vessels. -Vitelline duct and vitelline vessels. -Connection between intraembryonic and extra- embryonic coelom. Dr. Sherif Fahmy
  • 6. Primitive umbilical cord: - Expansion of amniotic cavity, leads to elongation of umbilical cord. Contents: 1- Yolk sac and vitelline duct. 2- Connecting stalk with remnant of allantois. 3- Intestinal loop in its proximal part. 4- Umbilical and vitelline vessels. Dr. Sherif Fahmy
  • 7. Definitive umbilical cord: - Return of intestinal loop to abdominal cavity at 3rd month. -Obliteration of vitelline duct, allantois, extra- embryonic part of vitelline vessels. -Degeneration of one umbilical vein with persistence of other vein and 2 umbilical arteries. -Transformation of mesoderm of connecting stalk into wharton’s jelly.
  • 9. Embryonic disc with removed ectoderm Dr. Sherif Fahmy
  • 17. • Abnormalities of Umbilical Cord • 1- Short cord: leads to premature separation of placenta. • 2- Long cord: It may encircle neck of fetus and may form true knots. • 3- Congenital umbilical hernia (omphalocele): the cord contains coils of intestine. • 4- Presence of one umbilical artery. • 5- Abnormal attachment of the cord: –Marginal attachment (battledore) –Through membranes (velamentous). Dr. Sherif Fahmy
  • 22. Types of TWINS Dizygotic (Fraternal) twins: - It is the commonest type as it represent 2/3 of twins and 7 – 11 / 1000 births. - Fertilization of 2 separate ova. - Each embryo has its own placenta, chorion and amniotic cavity. - Twins are non-identical and may of same sex or different. Dr. Sherif Fahmy
  • 23. Monozygotic (Identical) twins: Developed from division of a fertilized ovum. Twins of this type are identical and of same sex. Its incidence is 0.3 – 0.4 % Division may occure at 3 different stages: 1- At morula stage: Twins has separate amnion, chorion and placentae (as in dizygotic). 2- At blastocyst stage: due to division of inner cell mass. Twins has separate amniotic cavity but single chorion and placenta. 3- At embryonic disc: Midline division of the embryonic disc. Twins has common amniotic cavity, common chorion and common placenta . Dr. Sherif Fahmy
  • 25. SIAMESE (CONJOINED) TWINS • Fused monozygotic twins that occurs due to incomplete separation of emberyonic disc. They could be either: Craniopagus: Fusion between 2 heads. Thoracopagus: Fusion at thoracic region. Pygopagus: Fusion at the pelvic region. Dr. Sherif Fahmy
  • 29. 1- Enviromental Factors • Infectious Agents: Viruses, Bacteria and parasites. • Radiations: X-ray, Gamma and atomic radiation. • Drugs & chemicals: e.g. antiepileptic drugs, vit. A, Alcohol • Maternal diabetes: Dr. Sherif Fahmy
  • 31. 1- Numerical Chromosomal Anomalies A-Autosomal: • A- Triosomy 21 (Down or Mongolism). • Each cell contains 47 chomosomes (45 + XX or XY). • B- Triosomy 13, 15, 17 & 18. Dr. Sherif Fahmy
  • 32. B- Sex Numerical Chromosomal Anomalies • 1- Klinefelter syndrome: (44 + XXy) Due to non-disjunction of X chromosome. Male case suffers from infertility and gynecomastia. • 2- Turner syndrome: (44 + X0) Due to non-disjunction of X chromosome. Female case suffers from gonadal dysgenesis, short staure and neck skin fold Dr. Sherif Fahmy
  • 33. 2- Structural Chromosomal Anomaly • A- Cri-du-Chat Syndrome. Due to partial deletion of short arm of chromosome 5 (cat-like cry, microcephaly and mental retardation). • B- Angelman Syndrome. Partial deletion of long arm of chromosome 15 (mental retardation, poor motor development and prolonged period of laughter. Dr. Sherif Fahmy
  • 35.
  • 36. Cri du Chat Syndrome
  • 39. A Child of Alcoholic Mother
  • 40. A Child of A Mother Treated by Antiepileptic drug
  • 41. A Child of A Mother Treated with Antithyroid drug
  • 42. A Child of A mother Exposed to Rubella Infection
  • 43. External Appearance of the Embryo (4th – 8th week) At the embryonic period (4th – 8th week), human shape becomes easily identified. -Head, body and limb buds are easily identified. -Eyes, nose and ears are seen.
  • 44. C-R length in mms Age of embryo in weeks 5 – 8 5 10 – 14 6 17 – 22 7 28 – 30 8
  • 46. C-R length in cm Age of embryo in months 5 – 8 cm 3rd month 18 cm 5th month 36 cm Full term fetus at birth
  • 47. Relative size of head to body: -At the beginning of the 3rd month, the head is ½ the CR length. -At the beginning of the 5th month, the head is 1/3 the CH length. -At birth, the head is ¼ of CH length. Weight growth: -At the end of 5th month, the weight is ½ kg. -At the 7th month, the weight is 1.75 kg. -At full term, the weight is 3.5 kg.
  • 48. Changes in external features: -Face becomes human looking. -Limbs become longer. -External genitalia are differentiated at 12th week. -Lanugo hair covers the fetus since the 4th month. -The skin is wrinkled till the end of 6th month. -Testes descend to scrotum just before birth. -Skin is covered by fatty substance called vernix caesosa. Fetal movement: It is clearly recognized since the 5th month.
  • 49. The End & Beginning With my best wishes Dr. Sherif Fahmy