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Novel mutation in the SETD1A gene in a newborn patient associating with congenital airway and heart defeats: A case report
Congenital malformations are commonly associated with genetic disorders in infants and children. PATIENT CONCERNS: A 13-day-old male infant was admitted to our hospital presenting with aggravated dyspnea and characteristic facial and body features. Examinations during hospitalization found congenita...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063285/ https://www.ncbi.nlm.nih.gov/pubmed/37000069 http://dx.doi.org/10.1097/MD.0000000000033449 |