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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