[PDF][PDF] Anderson-Fabry disease: a case report with MR, CT, and cerebral angiography
R Moumdjian, D Tampieri… - … : American Journal of …, 1989 - Am Soc Neuroradiology
Discussion Anderson-Fabry disease (angiokeratoma corporis diffusum) is a form of
sphingolipidosis inherited as an X-linked recessive trait. Female carriers, however, show an …
sphingolipidosis inherited as an X-linked recessive trait. Female carriers, however, show an …
Anderson-Fabry's disease: neuropathological and neurochemical investigation
F Tagliavini, V Pietrini, F Gemignani, A Lechi… - Acta …, 1982 - Springer
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 …
disease is described. The clinical course mainly consisted of repeated icuts with major …
Anderson-Fabry disease: a histopathological study of three cases with observations on the mechanism of production of pain
P Kahn - Journal of Neurology, Neurosurgery & Psychiatry, 1973 - jnnp.bmj.com
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 …
presented and pathological changes in the central and peripheral nervous systems are …
Anorexia, weight loss, and diarrhea as presenting symptoms of angiokeratoma corporis diffusum (Fabry-Anderson's disease)
GF Nelis, GJA Jacobs - Digestive diseases and sciences, 1989 - Springer
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 …
sphingolipidosis with a systemic character and occurs in 2–5 per million births (1–3). The …
Renal transplantation in Anderson-Fabry disease
M Clement, PM Monkhouse… - Journal of the Royal …, 1982 - journals.sagepub.com
Anderson-Fabry disease (angiokeratoma corporis diffusum) is a rare, sex-linked, recessive
disorder of sphingolipid metabolism. The disease is characterized by a deficiency or …
disorder of sphingolipid metabolism. The disease is characterized by a deficiency or …
Anderson-Fabry disease (angiokeratoma corporis diffusum universale).
KW Radcliffe, BA Evans - Genitourinary medicine, 1990 - ncbi.nlm.nih.gov
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 …
due to an X-linked recessive inherited deficiency of the enzyme a-galoctosidase A …
Peripheral nerve involvement in Fabry's disease
RS Kocen, PK Thomas - Archives of Neurology, 1970 - jamanetwork.com
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 …
of lipid metabolism which displays a sex-linked recessive transmission. In hemizygous male …
Renal involvement in Anderson-Fabry disease.
A Sessa, M Meroni, G Battini, M Righetti… - Journal of …, 2003 - europepmc.org
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 …
glycosphingolipid (GL) metabolism, caused by a deficiency of the activity of alpha …
[CITATION][C] Anderson-Fabry disease in children and adolescents
M Beck, C Whybra, K Wendrich, A Gal, M Ries - Rare Kidney Diseases, 2001 - karger.com
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 …
also the first symptoms of Fabry disease in females. They were described either as chronic …
Anderson-Fabry disease with cerebrovascular complications in two Italian families
W Borsini, G Giuliacci, F Torricelli, E Pelo… - Neurological …, 2002 - Springer
We describe four patients with cerebrovascular complications from two unrelated Italian
families with Anderson-Fabry disease. Clinical examination, neuroimaging (MRI) …
families with Anderson-Fabry disease. Clinical examination, neuroimaging (MRI) …
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