| Literature DB >> 406603 |
Abstract
The clinical features, diagnosis management, aetiology and inheritance of angiokeratoma corporis diffusum (Fabry's disease) are discussed and the literature reviewed. The treatment and knowledge generally of this rare condition have not greatly improved in 75 years.Entities:
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Year: 1977 PMID： 406603 PMCID： PMC2496609 DOI： 10.1136/pgmj.53.616.78
Source DB: PubMed Journal: Postgrad Med J ISSN： 0032-5473 Impact factor: 2.401