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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Published in | International Journal of Medical and Surgical Sciences Vol. 10; no. 3 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Spanish |
Published |
2023
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Subjects | |
Online Access | Get full text |
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