Discussion Anderson-Fabry disease (angiokeratoma corporis diffusum) is a form of
sphingolipidosis inherited as an X-linked recessive trait. Female carriers, however, show an …

A clinical, neuropathological and neurochemical study of a case of Anderson-Fabry's
disease is described. The clinical course mainly consisted of repeated icuts with major …

A clinical review and histopathological study of three cases of Anderson-Fabry disease is
presented and pathological changes in the central and peripheral nervous systems are …

Fabry-Anderson's disease or angiokeratoma corporis diffusum (ACD) is an X-linked
sphingolipidosis with a systemic character and occurs in 2–5 per million births (1–3). The …

Anderson-Fabry disease (angiokeratoma corporis diffusum) is a rare, sex-linked, recessive
disorder of sphingolipid metabolism. The disease is characterized by a deficiency or …

First described by the two eponymous dermatolog-ists in 1898, Anderson-Fabry disease is
due to an X-linked recessive inherited deficiency of the enzyme a-galoctosidase A …

ANGIOKERATOMA corporis diffusum or Fabry's disease is a genetically determined disorder
of lipid metabolism which displays a sex-linked recessive transmission. In hemizygous male …

Anderson-Fabry disease (AFd) is a rare X-linked lisosomal storage disorder of
glycosphingolipid (GL) metabolism, caused by a deficiency of the activity of alpha …

Results As often seen in affected males, recurrent burning sensations in the extremities were
also the first symptoms of Fabry disease in females. They were described either as chronic …

We describe four patients with cerebrovascular complications from two unrelated Italian
families with Anderson-Fabry disease. Clinical examination, neuroimaging (MRI) …