2026-05-12T05:45:14Z https://www.peertechzpublications.org/oai-pmh

oai:www.peertechzpublications.org:10.17352/2640-7876.000017 2019-11-12 PTZ.GJRD:VOL4

Gottron’s acrogeria and peliosis hepatis Gloria Cobo Ramírez Monica Lopez Rodriguez Andres Gonzalez Garcia Marta Rosas Cancio-Suarez Luis Adrian ViteriLuis Manzano Espinosa<p>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.</p> Global Journal of Rare Diseases - Peertechz Publications 2019-11-12 Case Report https://doi.org/10.17352/2640-7876.000017 en Copyright © Gloria Cobo Ramírez et al.