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fabry-anderson disease (3) 3
lysosomal storage disease (3) 3
diagnosis (2) 2
glycosphingolipids (2) 2
humans (2) 2
male (2) 2
physiopathology (2) 2
acroparaesthesia (1) 1
adult (1) 1
agalsidase-beta (1) 1
alpha-galactosidase (1) 1
alpha-galactosidase - analysis (1) 1
alpha-galactosidase - biosynthesis (1) 1
alpha-galactosidase - genetics (1) 1
alpha-galactosidase - therapeutic use (1) 1
alpha-galactosidase deficiency (1) 1
alpha-galactosidase-a (1) 1
alpha-n-acetylgalactosaminidase - therapeutic use (1) 1
amelogenesis imperfecta - complications (1) 1
anderson–fabry disease (1) 1
angiokeratoma corporis diffusum (1) 1
anorexia - etiology (1) 1
antibody-formation (1) 1
carrier (1) 1
case studies (1) 1
chromosomes, human, x - genetics (1) 1
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corneal verticillata (1) 1
diarrhea - etiology (1) 1
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déficit de α-galactosidasa (1) 1
endothelium, vascular - enzymology (1) 1
enfermedad de depósito lisosomal (1) 1
enfermedad de fabry-anderson (1) 1
enzyme replacement therapy (1) 1
fabry disease - complications (1) 1
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feeding and eating disorders - etiology (1) 1
gastroenterology & hepatology (1) 1
kidney - enzymology (1) 1
lysosomes - enzymology (1) 1
medical/surgical (1) 1
medicine (1) 1
medicine, general & internal (1) 1
myocardium - enzymology (1) 1
organ specificity (1) 1
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Revista Médica del Hospital General de México, ISSN 0185-1063, 2016, Volume 81, Issue 4, pp. 243 - 247
Abstract Anderson–Fabry disease is the second most common lysosomal storage disease after Gaucher disease. It is an X-linked lysosomal disorder that causes a... 
Medical/Surgical | alpha-Galactosidase deficiency | Déficit de α-galactosidasa | Anderson–Fabry disease | Enfermedad de Fabry-Anderson | Lysosomal storage disease | Enfermedad de depósito lisosomal
Journal Article
Revista de Investigacion Clinica, ISSN 0034-8376, 05/2011, Volume 63, Issue 3, pp. 314 - 321
Journal Article
Indian Journal of Dermatology, Venereology and Leprology, ISSN 0378-6323, 1995, Volume 61, Issue 4, pp. 218 - 219
A case of angiokeratoma corporis diffusum having some classical features with dilatation of retinal vessels, but without urinary signs of renal involvement, is... 
acroparaesthesia | Fabry-Anderson disease | corneal verticillata
Journal Article
Digestive Diseases and Sciences, ISSN 0163-2116, 1989, Volume 34, Issue 11, pp. 1798 - 1800
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... 
angiokeratoma corporis diffusum | Fabry-Anderson's disease | GASTROENTEROLOGY & HEPATOLOGY | Feeding and Eating Disorders - etiology | Weight Loss | Humans | Anorexia - etiology | Fabry Disease - complications | Adult | Diarrhea - etiology | Family | Male | Amelogenesis Imperfecta - complications | Case studies | Diagnosis | Complications | Fabry's disease
Journal Article
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