Sanjad-sakati syndrome in omani children

Bushra Rafique, Saif Al-Yaarubi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)227-229
Number of pages3
JournalOman Medical Journal
Volume25
Issue number3
DOIs
Publication statusPublished - Jul 2010

ASJC Scopus subject areas

  • Medicine(all)

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