Umbilical Cord (General Embryology)

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UMBILICA L CORD Dr. Sherif Fahmy

Transcript of Umbilical Cord (General Embryology)

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UMBILICAL CORD

Dr. Sherif Fahmy

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Morphology of Umbilical CordIt 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.– Allows free mobility of the fetus.

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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.

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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.

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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.

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Development

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Embryonic disc with removed ectoderm

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• 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).

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TwinsDr. Sherif Fahmy

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Types of TWINSDizygotic (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.

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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 .

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Morula

stageEmbryonic Disc StageEarly

blastcyste

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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.

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Conjoined Twines

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Birth DefectsDr. Sherif Fahmy

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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:

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Chromosomal

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1- Numerical Chromosomal AnomaliesA-Autosomal:• A- Triosomy 21 (Down or Mongolism).• Each cell contains 47 chomosomes (45 + XX or

XY).• B- Triosomy 13, 15, 17 & 18.

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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

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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.

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Down Syndrome

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Cri du Chat Syndrome

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Turner Syndrome

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Achondroplasia

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A Child of Alcoholic Mother

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A Child of A Mother Treated by Antiepileptic drug

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A Child of A Mother Treated with Antithyroid drug

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A Child of A mother Exposed to Rubella Infection

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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.

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C-R length in mms Age of embryo in weeks

5 – 8 5

10 – 14 6

17 – 22 7

28 – 30 8

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Fetal Period

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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

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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.

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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.

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The End & Beginning

With my best wishes Dr. Sherif

Fahmy