Description

Focal dilatation of an artery
Placenta where the lobes are nearly equal in size and the cord inserts into the bridge that connects them
Fatal condition associated with multiple congenital anomalies and absence of the umbilical cord
Attachment of the placental membranes to the fetal surface of the placenta
Bending, twisting, and bulging of the umbilical cord vessels mimicking a knot in the umbilical cord
Periumbilical abdominal wall defect, typically right of the normal cord insertion where bowel floats freely
Condition characterized by multiple complex fetal anomalies and a short umbilical cord
Occurs when the umbilical cord inserts at the placental margin
A thickened placenta
Linear extra-embryonic tissue that projects into the amniotic cavity with no restriction of fetal movement. (Asherman's syndrome)
Intraplacental area of hemorrhage and clot
This occurs as a result of the fetus passing through loops of cord.
Central abdominal wall defect at the umbilicus where abdominal organs are contained by a covering membrane consisting of peritoneum, wharton's jelly, and amnion
Placental Tissue that partially covers the internal cervical os
Chorionic Villi that infiltrate up to or beyond the uterine serosa
A bladder with color Doppler placed on it that shows color around both sides is indicative of what?
When the umbilical cord has extended through the dilated cervical canal
Abnormally formed organs
When one or both testis fail to descend from the abdomen into the scrotal sac
Abnormal position of fingers and toes
Congenital absence of one or both eyes
Malformation of an organ or structure
Complete exposure of the spinal cord due to lack of fusion
Central portion of the cerebellum between the hemispheres
Spinal defect where the meninges protrude
Increased orbital distance
Enlarged tongue extending beyond the aveolar ridge
Severely hypoplastic mandible or small chin
Second most common congenital malformation
Absent neural tissue, spinal defects, polyhydramnios
A rare congenital disorder in which there is a complete or partial absence of the corpus callosum
Which type of Holoprosencephaly is the worst?
A malformation that is a rare anomaly of the posterior fossa that consists of a marked cystic dilatation of the fourth ventricle, agenesis of of the cerebellar vermis, and elevated tentorium

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Placentas

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