Amputation, Congenital: From 1 Different Sources
The separation of a body part (usually a limb, finger, or toe) from the rest of the body, as a result of the part’s blood supply being blocked by a band of amnion (fetal membrane) in the uterus.
The affected part may be completely separated or show the marks of the “amniotic band” after birth.
(See also limb defects.)
Congenital deformities, diseases, etc. are those which are either present at birth, or which, being transmitted direct from the parents, show themselves some time after birth.... congenital
See ADRENOGENITAL SYNDROME and GENETIC DISORDERS.... congenital adrenal hyperplasia
Loss of a finger, toe, or limb through injury. (See also microsurgery.)... amputation, traumatic
See developmental hip dysplasia.... hip, congenital dislocation of
see transposition of the great vessels.... congenitally corrected transposition
an operation involving removal of an entire arm, including the scapula and clavicle. It is usually performed for soft tissue or bone sarcomas arising from the upper arm or shoulder. Compare hindquarter amputation.... forequarter amputation
an operation involving removal of an entire leg and part or all of the pelvis associated with it. It is usually performed for soft tissue or bone sarcomas arising from the upper thigh, hip, or buttock. Compare forequarter amputation.... hindquarter amputation
a hereditary condition (inherited as an autosomal *recessive) causing severe visual loss in infants. The *fundus usually appears to be normal when examined with an *ophthalmoscope, but marked abnormalities are found on the ERG (see electroretinography), usually with extinguished wave pattern. [T. Leber (1840–1917), German ophthalmologist]... leber’s congenital amaurosis
(CDH) herniation of the fetal abdominal organs into the fetal chest, which occurs in one in 2000–5000 live births. This leads to pulmonary *hypoplasia, which is the main cause of the associated high neonatal mortality. The risk of pulmonary hypoplasia is substantially greater where there is herniation of the liver into the thoracic cavity. CDH is commonly associated with additional structural abnormalities (cardiac, neural tube defects, and exomphalos), and the risk of chromosomal abnormality (*aneuploidy) is 10–20%. Demonstration of a fluid-filled bowel at the level of the heart on ultrasound is diagnostic.... congenital diaphragmatic hernia
(CDH) an abnormality present at birth in which the head of the femur is displaced or easily displaceable from the acetabulum (socket) of the ilium, which is poorly developed; it frequently affects both hip joints. CDH occurs in about 1.5 per 1000 live births, being more common in first-born girls, in breech deliveries, and if there is a family history of the condition. The leg is shortened and has a reduced range of movement, and the skin creases may be asymmetrical. All babies are routinely screened for CDH at birth and at developmental check-ups by gentle manipulation of the hip causing it to be reduced and dislocated with a clunk (see Barlow manoeuvre; Ortolani manoeuvre). The diagnosis is confirmed by X-ray or ultrasound scan. Treatment is with a special harness holding the hip in the correct position. If this is unsuccessful, the hip is reduced under anaesthetic and held with a plaster of Paris cast or the defect is corrected by surgery. Successful treatment of an infant can give a normal hip; if the dislocation is not detected, the hip does not develop normally and osteoarthritis develops at a young age.... congenital dislocation of the hip