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- Renal dysplasia-limb defects syndrome - Renal dysplasia-limb defects syndrome (RL syndrome), also known as Ulbright Hodes syndrome is a very rare syndrome. The syndrome has been described in three infants, all of whom died shortly after birth.
- Hallermann-Streiff syndrome - The Hallermann-Streiff syndrome (also known as the François Dyscephalic Syndrome, Hallermann-Streiff-François syndrome, Oculomandibulodyscephaly with hypotrichosis and the Oculomandibulofacial Syndrome) is a disorder that effects the body's stature, head structure and hair growth. Patients with this syndrome are shorter than the average person and may not develop hair in many places, including in the ...
- Beals syndrome - Beals syndrome (Congenital contractural arachnodactyly, Beals-Hecht syndrome) is a rare congenital connective tissue disorder. Beals syndrome has only recently been described as a syndrome distinct from Marfan's Syndrome.
- Fetal trimethadione syndrome - Fetal trimethadione syndrome (also known as paramethadione syndrome, German syndrome, tridione syndrome, among othersAdditional names include trimethadione embryopathy and trimethadione syndrome.) is a set of birth defects caused by the administration of the anticonvulsants trimethadione (also known as Tridione) or paramethadione to epileptic mothers during pregnancy.
- POEMS syndrome - POEMS syndrome (also known as Crow-Fukase syndrome, Takatsuki disease, or PEP syndrome) is a rare medical syndrome named for its main clinically recognizable features: Polyneuropathy (peripheral nerve damage), Organomegaly (abnormal enlargement of organs), Endocrinopathy (damage to hormone-producing glands)/Edema, M-protein (an abnormal antibody) and Skin abnormalities (including hyperpigmentation and hypertrichosis).