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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Bibliografske podrobnosti
izdano v:Iran J Med Sci
Main Authors: Shankar, Binoy, Bhutia, Euden, Kumar, Dinesh, Kishore, Sunil, Das, Shakti Pad
Format: Artigo
Jezik:Inglês
Izdano: Iranian Journal of Medical Sciences 2017
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5523052/
https://ncbi.nlm.nih.gov/pubmed/28761211
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