familial atrophia maculosa varioliformis cutis: first case report from the indian subcontinent with pedigree analysis

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ID: 196647
2012
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Ranked #113 of 318 articles by views in crystallization of organic compounds: an industrial perspective

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Abstract
Familial atrophia maculosa varioliformis cutis is a very rare disorder with less than 28 cases being reported in the literature worldwide and remains a mystery both as far as genetics and the virtue of its pathogenesis is concerned. We present a case of mother and son, both having this disorder with presentations unique in terms of sites involved and try to draw a five generations pedigree chart for the same. We further support its inheritance pattern as autosomal dominant. Also, we propose oral isotretinoin as an effective treatment modality for the same.
Reference Key
goyal2012indianfamilial Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Tarang Goyal;Anupam Varshney;S K Bakshi
Journal crystallization of organic compounds: an industrial perspective
Year 2012
DOI
10.4103/0378-6323.93637
URL
Keywords Keywords not found

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