Fabry's disease manifesting as familial angiokeratoma corporis diffusum in an indian family – A rare occurrence!
Fabry's disease is a rare X-linked dermatosis, resulting from alpha-galactosidase deficiency and presents with both cutaneous (angiokeratoma, acral paresthesia, and hypohidrosis) and extracutaneous manifestations (ocular, cardiac, renal, and neurological). We report two brothers age 16 and 14 years...
Sábháilte in:
| Príomhchruthaitheoirí: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Wolters Kluwer Medknow Publications
2020-01-01
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| Sraith: | Indian Journal of Paediatric Dermatology |
| Ábhair: | |
| Rochtain ar líne: | http://www.ijpd.in/article.asp?issn=2319-7250;year=2020;volume=21;issue=4;spage=319;epage=322;aulast=Kaur |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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