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Bookmark or Share- Weaver syndrome - WikipediaWeaver syndrome is an extremely rare autosomal dominant genetic disorder associated with rapid growth beginning in the prenatal period and continuing through the toddler and youth years. It is characterized by advanced osseous maturation and distinctive craniofacial, skeletal and neurological abnormalities. [ 1 ]
- Orphanet: Weaver syndromeWeaver syndrome (WVS) is a rare, multisystem disorder characterized by tall stature, a typical facial appearance (hypertelorism, retrognathia) and variable intellectual disability. Additional features may include camptodactyly, soft doughy skin, umbilical hernia, and a low hoarse cry.
- Weaver syndrome - National Organization for Rare DisordersWeaver syndrome (WVS) is a rare, multisystem disorder characterized by tall stature, a typical facial appearance (hypertelorism, retrognathia) and variable intellectual disability. Additional features may include camptodactyly, soft doughy skin, umbilical hernia, and a low hoarse cry.
- Weaver syndrome - MedlinePlusWeaver syndrome is a condition that involves tall stature with or without a large head size (macrocephaly), a variable degree of intellectual disability (usually mild), and characteristic facial features.
- Weaver Syndrome - Cleveland ClinicWeaver syndrome, also called Weaver-Smith syndrome, is a genetic condition that causes bone overgrowth. The condition may also cause changes to the shape and appearance of your face and the size of your head.
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