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Phocomelia is a congenital condition that involves malformations of human arms and legs which result in a flipper-like appendage. [1] [2] A prominent cause of phocomelia is the mother being prescribed the use of the drug thalidomide during pregnancy; however, the causes of most cases are to be determined.
The following is a list of symptoms that have been associated with Roberts syndrome: [citation needed] Bilateral symmetric tetraphocomelia- a birth defect in which the hands and feet are attached to shortened arms and legs; Prenatal growth retardation An example of a severely affected Roberts syndrome Patient
One class of congenital limb deformities, limb reduction defects, occurs when one or more limbs are undersized or missing parts. The prevalence of these defects in the United States is approximately 1 in 1900 births. [2] This category includes amelia, ectrodactyly, radial dysplasia, and phocomelia among others. These defects are more likely to ...
Birth defects are divided into two main types: structural disorders in which problems are seen with the shape of a body part and functional disorders in which problems exist with how a body part works. [3] Functional disorders include metabolic and degenerative disorders. [3] Some birth defects include both structural and functional disorders. [3]
Fetal hydantoin syndrome, also called fetal dilantin syndrome, is a group of defects caused to the developing fetus by exposure to teratogenic effects of phenytoin. Dilantin is the brand name of the drug phenytoin sodium in the United States, commonly used in the treatment of epilepsy .
Sierra Samuels, who was a nurse at Jackson Memorial Hospital in Miami, shared photos of a newborn with a birth defect that causes the baby's intestines to protrude from the body.
Scheana Shay just gave birth, and she’s already opening up about the details of her labor, including a serious medical condition. Pregnant Scheana Shay Shows Bare Baby Bump Before Going Into ...
Caudal regression syndrome, or sacral agenesis (or hypoplasia of the sacrum), is a rare birth defect. It is a congenital disorder in which the fetal development of the lower spine—the caudal partition of the spine—is abnormal. [1] It occurs at a rate of approximately one per 60,000 live births. [2]