Holt-Oram Syndrome: A Rare Variant

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are b...

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Detalles Bibliográficos
Autores principales: Shankar, Binoy, Bhutia, Euden, Kumar, Dinesh, Kishore, Sunil, Das, Shakti Pad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Journal of Medical Sciences 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523052/
https://www.ncbi.nlm.nih.gov/pubmed/28761211

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523052/
https://www.ncbi.nlm.nih.gov/pubmed/28761211

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