Sanjad-Sakati Syndrome in Omani children.
Authors:
- Saif Al-YaarubiSASaif Al-Yaarubi
- 1 July 2010
- Vol. 25 (3) , 227-9
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.Keywords
This publication has 7 references indexed in Scilit:
- Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in KuwaitEastern Mediterranean Health Journal, 2009
- Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features-another case of this new syndromeClinical Genetics, 2008
- Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43Journal of Medical Genetics, 2000
- Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43The American Journal of Human Genetics, 1998
- Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomaliesAmerican Journal of Medical Genetics, 1994
- A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.Archives of Disease in Childhood, 1991
- Short stature, mental retardation, and hypoparathyroidism: a new syndrome.Archives of Disease in Childhood, 1990