Necrosis isquémica intestinal transmural en un paciente con síndrome de Kabuki: un reporte de caso

Kabuki syndrome (KS) is a rare genetic disorder in which mutations in the KMT2D or KDM6A genes result in a wide spectrum of clinical manifestations including development and growth delay; intellectual dysfunction; craniofacial dysmorphism; and various systemic structural and functional defects. We p...

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Bibliographic Details
Published inInternational Journal of Medical and Surgical Sciences Vol. 10; no. 3
Main Authors Dragustinovis Hinojosa, Gustavo, Mendoza, Humberto, Muñoz Maldonado, Gerardo Enrique, Méndez, Néstor, Gutiérrez González, Jorge Aurelio, Guerrero Zertuche, Juventino Tadeo
Format Journal Article
LanguageSpanish
Published 2023
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