HOLT-ORAM SYNDROME. CLINICAL OBSERVATION FROM THE CARDIOLOGY DEPARTMENT OF THE RABAT CHILDREN'S HOSPITAL
*S. Kebabi, L. Chrakh, L. Chtouki, F. Jabourik and A. Bentahila
ABSTRACT
Holt-Oram syndrome is a rare cardiomelic syndrome with autosomal dominant inheritance. It is clinically characterized by upper limb malformations involving the radial segment, variable rhythm disturbances and congenital heart disease. We report a case, in a 6-month-old patient, revealed by cyanosis and dyspnea on exertion.
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