Sanjad-Sakati syndrome in a Tunisian child
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference25 articles.
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3. Mutation in the TBCE gene is associated with hypoparathyroidism-retardation-dysmorphism syndrome featuring pituitary hormone deficiencies and hypoplasia of the anterior pituitary and the corpus callosum;Padidela;J Clin Endocrinol Metab,2009
4. Partial agenesis of corpus callosum in Sanjad-Sakati syndrome (p-ACC);Al Ghasab;Can J Neurol Sci,2012
5. Neurological manifestations in children with Sanjad-Sakati syndrome;Elhassanien;Int J Gen Med,2013
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1. Homozygous TBCE Gene Mutation c.155-166del in a Libyan Patient with Sanjad-Sakati Syndrome: Same Gene Mutation Responsible in All Arab Ethnic Patients;Journal of Pediatric Genetics;2022-06-15
2. Dental Management of a Tunisian Child with Sanjad-Sakati Syndrome;Case Reports in Dentistry;2022-04-22
3. Oral Facial Manifestations of Sanjad–Sakati Syndrome: A Literature Review;Children;2022-03-22
4. Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad–Sakati syndrome;Jornal de Pediatria;2020-01
5. Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad‐Sakati syndrome;Jornal de Pediatria (Versão em Português);2020-01
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