FABRY DISEASE
\fˈabɹi dɪzˈiːz], \fˈabɹi dɪzˈiːz], \f_ˈa_b_ɹ_i d_ɪ_z_ˈiː_z]\
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Lysosomal storage disease caused by a deficiency of alpha-galactosidase A and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems. The disease is X-linked and is characterized by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems.
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