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Literature DB >> 22043344

Sanjad-Sakati Syndrome in Omani children.

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.

Entities: Chemical Disease Gene Species

Year: 2010 PMID： 22043344 PMCID： PMC3191633 DOI： 10.5001/omj.2010.63

Source DB: PubMed Journal: Oman Med J ISSN： 1999-768X

7 in total

1. Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43.

Authors: T E Kelly; S Blanton; R Saif; S A Sanjad; N A Sakati
Journal: J Med Genet Date: 2000-01 Impact factor: 6.318

2. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Authors: S A Sanjad; N A Sakati; Y K Abu-Osba; R Kaddoura; R D Milner
Journal: Arch Dis Child Date: 1991-02 Impact factor: 3.791

3. Short stature, mental retardation, and hypoparathyroidism: a new syndrome.

Authors: R J Richardson; J M Kirk
Journal: Arch Dis Child Date: 1990-10 Impact factor: 3.791

4. Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features--another case of this new syndrome.

Authors: M A Kalam; W Hafeez
Journal: Clin Genet Date: 1992-09 Impact factor: 4.438

5. Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies.

Authors: D Marsden; W L Nyhan; N O Sakati
Journal: Am J Med Genet Date: 1994-09-01

6. Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.

Authors: R Parvari; E Hershkovitz; A Kanis; R Gorodischer; S Shalitin; V C Sheffield; R Carmi
Journal: Am J Hum Genet Date: 1998-07 Impact factor: 11.025

7. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.

Authors: K K Naguib; S A Gouda; A Elshafey; F Mohammed; L Bastaki; A S Azab; S A Alawadi
Journal: East Mediterr Health J Date: 2009 Mar-Apr Impact factor: 1.628

7 in total

8 in total

Sanjad-Sakati Syndrome in Omani children.

1. Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43.

2. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

3. Short stature, mental retardation, and hypoparathyroidism: a new syndrome.

4. Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features--another case of this new syndrome.

5. Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies.

6. Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.

7. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.

Review 1. Endocrinological Manifestations of Sanjad-Sakati Syndrome.

2. Sanjad-Sakati Syndrome in Sudanese children.

3. New Ocular Associations in Sanjad-Sakati Syndrome: Case report from Oman.

4. Dental Management of a Tunisian Child with Sanjad-Sakati Syndrome.

Review 5. Oral Facial Manifestations of Sanjad-Sakati Syndrome: A Literature Review.

6. Sanjad-sakati syndrome dental management: a case report.

7. Impact of intercurrent illness on calcium homeostasis in children with hypoparathyroidism: a case series.

8. Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome.