Premium
Two Cases of Fabry's Disease: A Hemizygote with a Point Mutation in the α‐Galactosidase A Gene and His Relative
Author(s) -
Inaoki Makoto,
Otsuki Norio,
Ishise Syozo,
Ueda Yoshimichi,
Sakuraba Hitoshi
Publication year - 1992
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/j.1346-8138.1992.tb03266.x
Subject(s) - angiokeratoma , medicine , telangiectases , fabry disease , missense mutation , hypertrophic cardiomyopathy , pathology , cardiology , telangiectasia , biology , gene , mutation , genetics , disease
A 34‐year‐old Japanese male had leg pain, edema of the legs, hypohidrosis, whorl‐like opacities of the bilateral cornea, bilateral subcapsular cataracts, and chest discomfort on exercise. He had no characteristic angiokeratomas but did have telangiectases. The electrocardiogram revealed high voltage. The echocardiogram revealed mild mitral regurgitation. The α‐galactosidase A activity in cultured lymphoblasts was deficient (0.5 nmol/h/mg protein). Electron microscopic examination of the skin revealed lamellar cytoplasmic inclusions in the endothelial cells, pericytes, and fibroblasts. He had a G—A transition at nucleotide 982 in the coding sequence of the α‐galactosidase A gene which resulted in a glycine to arginine amino acid substitution at residue 328. His uncle also had leg pain, edema of the legs, hypohidrosis, and chest pain on exercise. He had no characteristic angiokeratomas but did have telangiectases. Cardiovascular examination revealed hypertrophic cardiomyopathy and stenoses of coronary arteries. Electron microscopic examination of the skin revealed lamellar cytoplasmic inclusions in the endothelial cells, pericytes, and fibroblasts.