Hand-foot-genital syndrome is a rare condition that affects the development of the hands and feet, the urinary tract, and the reproductive system. People ...

... Hartsfield-Bixler-Demyer syndrome HHES Holoprosencephaly and split hand/foot syndrome Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Holoprosencephaly, ...

... the HOXA13 gene have been found to cause hand-foot-genital syndrome. As its name suggests, this condition affects the ... may cause more severe signs and symptoms of hand-foot-genital syndrome than variants that lead to a nonfunctional version ...

... of the skin on the palms and soles (hand-foot syndrome); shortness of breath; and hair loss may also ...

... p53-competing protein Tests of TP63 PubMed ADULT SYNDROME SPLIT-HAND/FOOT MALFORMATION 4; SHFM4 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3 TUMOR PROTEIN p63; TP63 LIMB-MAMMARY ...

... these changes lead specifically to holoprosencephaly and split hand/foot in people with Hartsfield syndrome. More About This Health Condition Many FGFR1 gene ...

... it does not include lissencephaly. 17p13.3 duplication syndrome, also called split-hand/foot malformation with long bone deficiency or SHFLD3, is ...

... A16), which cause a viral infection known as hand, foot, and mouth disease, use the LIMP-2 protein. At least 20 mutations in the SCARB2 gene have been associated with action myoclonus–renal failure (AMRF) syndrome. This rare condition causes episodes of involuntary muscle ...

... lead to the characteristic “whistling face” appearance and hand, foot, ... of Freeman-Sheldon syndrome. A small number of people with Freeman-Sheldon ...