Hyperpigmented, hypertrichotic, and sclerodermoid plaques: An unusual variant of Muckle–Wells syndrome
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference7 articles.
1. The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations;Molho-Pessach;J Am Acad Dermatol,2008
2. Autosomal recessive plasma cell paniculitis with morphea-like clinical manifestation;Hamadah;J Am Acad Dermatol,2006
3. POEMS in childhood;Marina;Pediatr Dermatol,2006
4. Pigmented hypertrichotic dermatosis and insulin dependent diabetes: manifestations of a unique genetic disorder?;Prendiville;Pediatr Dermatol,2006
5. Muckle–Wells syndrome: report of six cases with hyperpigmented sclerodermoid skin lesions;El-Darouti;Int J Dermatol,2006
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. H syndrome: The first 79 patients;Journal of the American Academy of Dermatology;2014-01
2. The spectrum of radiological findings in H syndrome;Clinical Imaging;2013-03
3. Indurated, Dark, Hairy Plaques, with Arthritis and Deafness;Challenging Cases in Dermatology;2012-09-04
4. Expanding the clinical spectrum of SLC29A3 gene defects;European Journal of Medical Genetics;2010-09
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