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2017, Número 3

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Med Cutan Iber Lat Am 2017; 45 (3)


Mal de Meleda. Relato de dois casos numa família

Morais P, Peralta L, Garcia H, Oliveira M

Idioma: Español
Referencias bibliográficas: 19
Paginas: 232-236
Archivo PDF: 318.09 Kb.


RESUMEN

O Mal de Meleda é uma genodermatose rara, com padrão de hereditariedade autossómico recessivo, caracterizada por hiperqueratose difusa e transgressiva das regiões palmoplantares. Neste artigo apresentamos o caso de dois irmãos afectados por esta forma de queratodermia palmoplantar em contexto de consanguinidade entre os progenitores.


REFERENCIAS (EN ESTE ARTÍCULO)

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