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.
|الصفحات (من إلى)||227-229|
|دورية||Oman Medical Journal|
|المعرِّفات الرقمية للأشياء|
|حالة النشر||Published - يوليو 2010|
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