The Dorfman Chanarin syndrome - A very rare, autosomal recessive genetic disorder affecting fat metabolism (see lipidosis). The disease is congenital (present from birth).
It is characterized by ichthyosis (thickened, scaly skin); myopathy (degeneration of muscle), and sometimes also defects in vision and in hearing. Blood tests show abnormal white blood cells containing vacuoles (tiny spaces) filled with fat.
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