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ISSN: 2640-7876
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Global Journal of Rare Diseases

    Abstract

    Open Access Case Report Article ID: GJRD-4-117

    Gottron’s acrogeria and peliosis hepatis

    Gloria Cobo Ramírez*, Monica Lopez Rodriguez, Andres Gonzalez Garcia, Marta Rosas Cancio-Suarez, Luis Adrian Viteri and Luis Manzano Espinosa

    We report the case of a 62-year-old woman with Gottron’s acrogeria and peliosis hepatis. Gottron’s acrogeria is a rare congenital disease characterized by atrophic acral skin with mottled hyperpigmentation and an aged appearance. It is mostly caused by a mutation in COL3A1 gene that leads to defective production of type III collagen.

    Keywords:

    Published on: Nov 12, 2019 Pages: 17-21

    Full Text PDF Full Text HTML DOI: 10.17352/2640-7876.000017
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