Kagami-Ogata Syndrome: Case Series and Review of Literature

Kagami-Ogata syndrome (KOS) (OMIM #608149) is a genetic imprinting disorder affecting chromosome 14 that results in a characteristic phenotype consisting of typical facial features, skeletal abnormalities including rib abnormalities described as “coat hanger ribs,” respiratory distress, abdominal wa...

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Detalles Bibliográficos
Autores principales: Sakaria, Rishika P., Mostafavi, Roya, Miller, Stephen, Ward, Jewell C., Pivnick, Eniko K., Talati, Ajay J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers, Inc. 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159623/
https://www.ncbi.nlm.nih.gov/pubmed/34055463
http://dx.doi.org/10.1055/s-0041-1727287

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159623/
https://www.ncbi.nlm.nih.gov/pubmed/34055463
http://dx.doi.org/10.1055/s-0041-1727287

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