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Results 1 - 5 of 5 for Muscular "dystrophy-dystroglycanopathy" congenital with brain eye anomalies "," type "a," 8
  1. Walker-Warburg syndrome 
    ... BRAIN AND EYE ANOMALIES), TYPE A, 10; MDDGA10 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8; MDDGA8 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  2. FKRP gene 
    ... found in a small number of people with congenital muscular dystrophy type 1C (MDC1C), which causes muscle weakness, brain abnormalities, and intellectual disability but usually does not affect the eyes. Rarely, mutations in the FKRP gene are associated ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  3. POMT2 gene 
    ... nerve cells (neurons) during early development. ... and abnormalities of the brain and eyes. Because of the severity of the problems caused ...
    https://medlineplus.gov/genetics/gene/pomt2 - Genetics
  4. FKTN gene 
    ... a condition that causes skeletal muscle weakness and brain and eye abnormalities. This form of congenital muscular dystrophy is seen almost exclusively in Japan. Virtually ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  5. CRPPA gene 
    ... form of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the brain and eyes. Because of the severity of the problems caused ...
    https://medlineplus.gov/genetics/gene/crppa - Genetics