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Elejalde syndrome: case presentation
JPAD-Journal of Pakistan Association of Dermatologists. 2014; 24 (4): 351-354
Dans Anglais | IMEMR | ID: emr-162421
ABSTRACT
Silvery hair and severe dysfunction of the central nervous system [Neuroectodermal melanolysosomal disease or Elejalde Syndrome] characterize this rare autosomal recessive syndrome. Main clinical features include silver-leaden hair, bronze skin after sun exposure, and neurologic involvement. Large granules of melanin unevenly distributed in the hair shaft are observed. Abnormal melanocytes and melanosomes and abnormal inclusion bodies in fibroblasts may be present. We report a 10-year-old girl with a silver-leaden [silvery] hair, bronze skin color on sun-exposed areas, generalized hypopigmentation of covered body parts and congenital seizures. The child was the elder of two children born of a consanguineous marriage. The younger sibling, a female neonate, had same clinical presentation
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Indice: Méditerranée orientale langue: Anglais Texte intégral: J. Pak. Assoc. Dermatol. Année: 2014

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Indice: Méditerranée orientale langue: Anglais Texte intégral: J. Pak. Assoc. Dermatol. Année: 2014