A Rare Variant and Unusual Presentation of Holt Oram Syndrome in a Child

Holt Oram syndrome is a rare genetically inherited disorder characterized by various skeletal abnormalities of the upper limb with an underlying structural heart defect. Family history and conduction defects may or may not be there. The diagnosis is often clinical; if the criteria are not fulfilled,...

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Detalles Bibliográficos
Autores principales: Reddy, Rasagnya M, Lakra, Mahaveer S, Meshram, Revat J, Taksande, Amar, Wanjari, Mayur B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Medical Education
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719589/
https://www.ncbi.nlm.nih.gov/pubmed/36475197
http://dx.doi.org/10.7759/cureus.31076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719589/
https://www.ncbi.nlm.nih.gov/pubmed/36475197
http://dx.doi.org/10.7759/cureus.31076

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