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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...
Autores principales: | Suriapperuma, Tharindi, Randeny, Shobhavi, Mettananda, Sachith |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
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 |
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