Angiokeratoma corporis diffusum universale

Introduction: Angiokeratoma corporis diffusum universale

Description of Angiokeratoma corporis diffusum universale

Angiokeratoma corporis diffusum universale: 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.
Source: Diseases Database

Angiokeratoma corporis diffusum universale: Related Topics

These medical condition or symptom topics may be relevant to medical information for Angiokeratoma corporis diffusum universale:

• Angiokeratoma corporis diffusum
• Angiokeratoma

Terms associated with Angiokeratoma corporis diffusum universale:

Terms Similar to Angiokeratoma corporis diffusum universale:

• Ceramide trihexosidase deficiency
• Fabry's disease
• Alpha-galactosidase A deficiency
• Anderson-Fabry disease

Source: Diseases Database

External links related to: Angiokeratoma corporis diffusum universale

• eMedicine - Fabry Disease - New Therapies : Article by Gregory Pastores, MD
• Fabry's Disease Information Page: National Institute of Neurological Disorders and Stroke (NINDS)
• Fabry disease - Genetics Home Reference
• Anderson-Fabry disease (www.whonamedit.com)
• eMedicine - Fabry Disease : Article by Zuzana Baranova, MD
• eMedicine - Fabry Disease : Article by Melissa Wasserstein, MD
• OMIM - FABRY DISEASE
• GeneReviews: Fabry Disease

Source: Diseases Database

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