{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T16:54:34Z","timestamp":1790787274863,"version":"4.1.0"},"reference-count":17,"publisher":"Mathematical Modelling and Numerical Simulation with Applications","issue":"03","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Pediatr Genet"],"published-print":{"date-parts":[[2024,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Sanjad-Sakati syndrome (SSS) (Online Mendelian Inheritance in Man 241410) is a rare autosomal recessive disorder also known as hypoparathyroidism-retardation-dysmorphism syndrome. It is characterized by congenital hypoparathyroidism, growth retardation, typical facial features, and variable developmental delay. SSS is caused due to mutations of the tubulin-specific chaperone E (TBCE) gene. In this article, we reported the first Libyan child of first parental consanguinity with SSS and whole exome sequencing results identified the homozygous missense variant c.155\u2013166del and it encodes p.(Ser52-Gly55del) (chr1:235564867) located in the TBCE gene, chromosome 1q42.3. In addition, the patient was also diagnosed with congenital hypothyroidism and presented with acquired bilateral cataract in the first year of life. Most likely, all Arab patients with SSS syndrome have the same TBCE gene mutation.<\/jats:p>","DOI":"10.1055\/s-0042-1744482","type":"journal-article","created":{"date-parts":[[2022,6,15]],"date-time":"2022-06-15T19:19:41Z","timestamp":1655320781000},"page":"211-214","source":"Crossref","is-referenced-by-count":3,"title":["Homozygous TBCE Gene Mutation c.155-166del in a Libyan Patient with Sanjad-Sakati Syndrome: Same Gene Mutation Responsible in All Arab Ethnic Patients"],"prefix":"10.53391","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7709-4514","authenticated-orcid":false,"given":"Millad","family":"Ghawil","sequence":"additional","affiliation":[{"name":"Pediatric Department, Faculty of Medicine, University of Tripoli, Tripoli University Hospital, Tripoli, Libya"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nesrin Ben","family":"Omar","sequence":"additional","affiliation":[{"name":"Division of Endocrinology, Pediatric Department, Faculty of Medicine, Tripoli University Hospital, University of Tripoli, Tripoli, Libya"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Milad","family":"Doggah","sequence":"additional","affiliation":[{"name":"Pediatric Department, Faculty of Medicine, University of Tripoli, Tripoli University Hospital, Tripoli, Libya"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"31409","published-online":{"date-parts":[[2022,6,15]]},"reference":[{"issue":"03","key":"ref1","first-page":"271A","article-title":"Congenital hypoparathyroidism with dysmorphic features: a new syndrome","volume":"23","author":"S A Sanjad","year":"1988","journal-title":"Pediatr Res"},{"issue":"02","key":"ref2","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1136\/adc.66.2.193","article-title":"A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features","volume":"66","author":"S A Sanjad","year":"1991","journal-title":"Arch Dis 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