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Homocystinuria syndrome: A rare genetic connective tissue disorder caused by an enzyme deficiency and characterized by dislocation of eye lens, malar flush and osteoporosis. More detailed information about the symptoms, causes, and treatments of Homocystinuria syndrome is available below.
See full list of 28 symptoms of Homocystinuria syndrome
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See full list of 10 occasional symptoms of Homocystinuria syndrome
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