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
Recent Cases of Holt oram syndrome
Browse recently discussed Holt oram syndrome cases by specialists476 Views
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Gandhi Medical College.
M.B.B.S.
AADESH MEDICAL COLLEGE
Associate Professor HEAD OF UNIT PAEDIATRIC
Dr SN Medical College Jodhpur
MD PAEDS
General Hospital Kanakapur
Md Pediatrics
MD Pediatrics
pediatrics
Shree Krishna Hospital
Resident
Pramukhswami Medical College
MD, INTERNAL MEDICINE
Private Practise
Md
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