Muckle-Wells syndrome: report of six cases with hyperpigmented sclerodermoid skin lesions

International Journal of Dermatology
Mohammad A El-DaroutiMona R E Abdel-Halim

Abstract

Muckle-Wells syndrome (MWS) is a rare syndrome, characterized by chronic recurrent urticaria, often combined with fever, chills, rigors, malaise, and arthralgia. Progressive sensorineural deafness, and, in approximately one third of the patients, amyloidosis of the kidneys as well as of other organs may occur. It was first described in 1962 by Muckle and Wells. Herein we describe six cases of MWS showing, in addition to the classic features of MWS, unique skin lesions that to the best of our knowledge have not been described before in association with MWS.

References

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Citations

Oct 28, 2008·Pediatric Dermatology·David R Berk, Susan J Bayliss
May 3, 2007·Nihon Rinshō Men'eki Gakkai kaishi = Japanese journal of clinical immunology·Tetsuo Kubota, Ryuji Koike
Mar 8, 2013·Clinical Imaging·Nurith HillerVered Molho-Pessach
Mar 20, 2010·International Journal of Pediatric Otorhinolaryngology·Deb Biswas, Nick Stafford
Aug 12, 2009·Journal of the American Academy of Dermatology·Mohammad A El-Darouti
Jul 21, 2009·Journal of the American Academy of Dermatology·Vered Molho-Pessach, Abraham Zlotogorski
Nov 1, 2013·Journal of the American Academy of Dermatology·Vered Molho-PessachAbraham Zlotogorski
Nov 5, 2016·Annals of the Rheumatic Diseases·Nienke M Ter HaarJoost Frenkel
Aug 15, 2018·International Journal of Dermatology·Antonina V KalmykovaOksana N Sulaieva
Feb 11, 2011·Anais Brasileiros De Dermatologia·Ana Francisca Junqueira Ribeiro PereiraLeandro Augusto Tanure
Jun 19, 2021·The World Allergy Organization Journal·Mario Sánchez-BorgesJose Antonio Ortega Martell

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