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Sanjad-Sakati Syndrome in Omani children
Bushra Rafique1, Saif Al-Yaarubi
1Department of Child Health, Sultan Qaboos University Hospital, Al Khod, Muscat, Sultanate of Oman.
Abstract:
Sanjad Sakati Syndrome is an Autosomal Recessive disorder found exclusively in people of Arabian origin. It was first reported from the Kingdom of Saudi Arabia in 1988. This is a report of a family with this rare disease in Oman. The syndrome comprises of congenital hypoparathyroidism, severe growth retardation, low IQ and typical facial features. Supportive treatment in the form of vitamin D and growth hormone is often offered to these children.
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