Ontology highlight
ABSTRACT:
SUBMITTER: Okada J
PROVIDER: S-EPMC5758919 | biostudies-literature | 2018 Mar
REPOSITORIES: biostudies-literature
Okada Jun J Hossain Mohammad Arif MA Wu Chen C Miyajima Takashi T Yanagisawa Hiroko H Akiyama Keiko K Eto Yoshikatsu Y
Molecular genetics and metabolism reports 20171222
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A (α-gal A), leading to the progressive accumulation of glycosphingolipids. Classical hemizygous males usually present symptoms, including pain and paresthesia in the extremities, angiokeratoma, hypo- or anhidrosis, abdominal pain, cornea verticillata, early stroke, tinnitus, and/or hearing loss, during early childhood or adolescence. Moreover, proteinuria, renal impairment, and cardiac hypertrophy ...[more]