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...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2020-01-01
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| Seri Bilgileri: | Indian Journal of Paediatric Dermatology |
| Konular: | |
| Online Erişim: | http://www.ijpd.in/article.asp?issn=2319-7250;year=2020;volume=21;issue=4;spage=319;epage=322;aulast=Kaur |
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