Literature DB >> 2818409

Familial localised scleroderma from Bangladesh: two case reports.

M A Wadud, B K Bose, T Al Nasir.   

Abstract

Familial scleroderma is rare. There have been few reported cases of familial scleroderma in medical literature. This report adds one more instance to the literature. Two members in one family had clinically and histologically established localised scleroderma (morphea). The hereditary aspect of the disease has not been well established. But this instance along with the previous documented instance suggest that genetic factor may play a role in the etiopathogenesis of the disease.

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Year:  1989        PMID: 2818409

Source DB:  PubMed          Journal:  Bangladesh Med Res Counc Bull        ISSN: 0377-9238


  4 in total

Review 1.  The Immunogenetics of Morphea and Lichen Sclerosus.

Authors:  Pooya Khan Mohammad Beigi
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

2.  Distinct autoimmune syndromes in morphea: a review of 245 adult and pediatric cases.

Authors:  Justin J Leitenberger; Rachael L Cayce; Robert W Haley; Beverley Adams-Huet; Paul R Bergstresser; Heidi T Jacobe
Journal:  Arch Dermatol       Date:  2009-05

Review 3.  Genetic counseling in the context of Bangladesh: current scenario, challenges, and a framework for genetic service implementation.

Authors:  Mohammad Jakir Hosen; Saeed Anwar; Jarin Taslem Mourosi; Sourav Chakraborty; Md Faruque Miah; Olivier M Vanakker
Journal:  Orphanet J Rare Dis       Date:  2021-04-09       Impact factor: 4.123

Review 4.  Morphea: progress to date and the road ahead.

Authors:  Laila Abbas; Adrienne Joseph; Elaine Kunzler; Heidi T Jacobe
Journal:  Ann Transl Med       Date:  2021-03
  4 in total

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