Holt oram syndrome
A rare, autosomal dominant inherited syndrome caused by mutations in the TBX5 gene. It is characterized by skeletal abnormalities in the upper limbs and heart abnormalities.
Disease Alternative Name
holt-oram syndrome
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Telangana State, Hyderabad.
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Dr SN Medical College Jodhpur
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pediatrics
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Private Practise
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Speaks English
205 Views