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2007, Número 4

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Dermatología Cosmética, Médica y Quirúrgica 2007; 5 (4)


Poroqueratosis: ¿Un mismo trastorno genético con diferente expresividad clínica?

López GL, Lammoglia L, Asz SD, Vega MME, Toussaint CS, Arenas R

Idioma: Español
Referencias bibliográficas: 39
Paginas: 239-248
Archivo PDF: 1328.51 Kb.


RESUMEN

Las poroqueratosis se manifiestan por el desarrollo de lesiones queratósicas en la piel con un cambio histológico característico, la presencia de laminilla cornoide. Se han descrito múltiples formas clínicas de la enfermedad pero son cinco las más reconocidas. El mecanismo de transmisión descrito en la mayoría de los casos es autosómico dominante.


REFERENCIAS (EN ESTE ARTÍCULO)

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