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Two Sisters with Mal de Meleda: Case Series Report. | LitMetric

Two Sisters with Mal de Meleda: Case Series Report.

Int J Appl Basic Med Res

Department of Pathology, Famagusta State Hospital, Famagusta, Cyprus.

Published: May 2022

Mal de Meleda (MDM) is a rare autosomal recessive type of palmoplantar keratoderma that is characterized by transgradient keratoderma with scleroatrophy, pseudoainhum around the fingers, and perioral erythema. Its features may also include lichenoid lesions, brachydactyly, and nail dystrophy. The disease has high morbidity and significantly impairs quality of life. Here, we describe two sisters with typical clinical presentations of MDM and a history of consanguinity between the parents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9215182PMC
http://dx.doi.org/10.4103/ijabmr.ijabmr_812_21DOI Listing

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