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ABCD syndrome
Overview
ABCD syndrome: A rare inherited condition characterized by albinism, deafness, a black lock of hair and intestinal abnormalities.
ABCD syndrome: A rare inherited condition characterized by albinism, deafness, a black lock of hair and intestinal abnormalities.
ACAD8 deficiency: An extremely rare metabolic disorder where the body is unable to metabolize certain proteins properly.
 See also: Mental retardation, Deafness, Angioma, Stroke, Aarskog syndrome
  
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