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Iranian Journal of Dermatology. 2005; 8 (2): 149-154
en Persa | IMEMR | ID: emr-71254

RESUMEN

Harlequin ichthyosis is one of the most severe congenital skin cornification disorders with an incidence rate of about 1 in 300,000 births and characteristic clinical features. We report two cases of harlequin ichthyosis [HI] or harlequin fetus [HF], which were products of consanguineous union. Clinical examination showed typical features of harlequin ichthyosis, with the presence of plaques with diamond-like configuration, external ear anomaly, severe ectropion and eclabium, and rigid semi flexion of limbs


Asunto(s)
Ictiosis Lamelar/epidemiología , Ictiosis Lamelar/diagnóstico , Enfermedades Cutáneas Papuloescamosas , Oído Externo/anomalías , Ectropión
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