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Porokeratosis of Mibelli: an uncommon genodermatosis
JPAD-Journal of Pakistan Association of Dermatologists. 2004; 14 (2): 93-95
en Inglés | IMEMR | ID: emr-66876
ABSTRACT
Porokeratosis of Mibelli is an uncommon, inherited, autosomal dominant disorder characterized by disordered epidermal keratinization and by a predisposition to develop malignant transformation. A case of this rare disorder with classical presentation in a teen aged boy is reported here, which was managed with topical retinoid, superficial chemical peeling and sunscreen lotion
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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Poroqueratosis Límite: Humanos / Masculino Idioma: Inglés Revista: J. Pak. Assoc. Dermatol. Año: 2004

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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Poroqueratosis Límite: Humanos / Masculino Idioma: Inglés Revista: J. Pak. Assoc. Dermatol. Año: 2004