Kagami–Ogata syndrome: a case report

BACKGROUND: Kagami–Ogata syndrome is a rare genetic imprinting disorder involving the 14q32.2 genomic location of chromosome 14. The estimated incidence is less than 1 per 1 million. Here we report a male neonate with Kagami–Ogata syndrome presenting with severe respiratory distress requiring mechan...

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Detalles Bibliográficos
Autores principales: Suriapperuma, Tharindi, Randeny, Shobhavi, Mettananda, Sachith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306061/
https://www.ncbi.nlm.nih.gov/pubmed/35864517
http://dx.doi.org/10.1186/s13256-022-03512-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306061/
https://www.ncbi.nlm.nih.gov/pubmed/35864517
http://dx.doi.org/10.1186/s13256-022-03512-6

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