Oral Facial Manifestations of Sanjad–Sakati Syndrome: A Literature Review
S Alghamdi - Children, 2022 - mdpi.com
Aim: To perform a comprehensive review of orofacial manifestations of Sanjad–Sakati
syndrome (SSS). Methods: A comprehensive electronic literature search was performed …
syndrome (SSS). Methods: A comprehensive electronic literature search was performed …
[HTML][HTML] Endocrinological manifestations of Sanjad-Sakati syndrome
M Bashar, M Taimur, FNU Amreek, KA Sayeed, A Tahir - Cureus, 2020 - ncbi.nlm.nih.gov
Abstract Sanjad-Sakati syndrome (SSS), also known as hypoparathyroidism-retardation-
dysmorphism (HRD) syndrome, is a very rare genetic disorder with an autosomal recessive …
dysmorphism (HRD) syndrome, is a very rare genetic disorder with an autosomal recessive …
[HTML][HTML] A staghorn calcium phosphate stone in a child with sanjad-sakati syndrome: an iatrogenic manifestation?
MA Alomar, MA Alghafees, RM Seyam, AS Aljurayyad… - Cureus, 2022 - ncbi.nlm.nih.gov
Sanjad-Sakati syndrome (SSS) is an autosomal recessive genetic condition, with the first
report discussing this condition presented in Saudi Arabia. This case report describes an …
report discussing this condition presented in Saudi Arabia. This case report describes an …
Hydrocephalus in Sanajd Sakati syndrome: a first clinical report
MA Elzain, M Alshammari, AA Jishi - Child's Nervous System, 2025 - Springer
Sanjad Sakati syndrome (SSS) is a rare autosomal recessive disorder seen among the Arab
population and is characterized by congenital hypothyroidism, growth retardation, and …
population and is characterized by congenital hypothyroidism, growth retardation, and …
Sanjad Sakati syndrome and sleep-disordered breathing: an undisclosed association
Abstract Background Sanjad Sakati syndrome (SSS) is a rare autosomal recessive genetic
disorder caused by mutation in TBCE (tubulin folding cofactor E) gene. Reported cases were …
disorder caused by mutation in TBCE (tubulin folding cofactor E) gene. Reported cases were …
[HTML][HTML] Autoimmune thyroiditis associated with Sanjad-Sakati syndrome: a call for regular thyroid screening
AM Anteet, ST Al Issa, AO Al-Ali… - Sudanese Journal of …, 2016 - ncbi.nlm.nih.gov
Abstract Sanjad-Sakati Syndrome (SSS) is a rare autosomal recessive disorder
characterized by congenital hypoparathyroidism, growth retardation and dysmorphism …
characterized by congenital hypoparathyroidism, growth retardation and dysmorphism …
[HTML][HTML] Sanjad-Sakati Syndrome Revealed by Hypocalcemic Convulsions
NEH Benchaib, A Elouali, A Sara, M Rkain… - Cureus, 2024 - pmc.ncbi.nlm.nih.gov
Sanjad-Sakati syndrome is an autosomal recessive disorder characterized by facial
dysmorphia, growth retardation, and congenital hypoparathyroidism. Epidemiologically, this …
dysmorphia, growth retardation, and congenital hypoparathyroidism. Epidemiologically, this …
Sanjad-Sakati Syndrome Revealed by Hypocalcemic Convulsions
BN El Houda, E Aziza, S Anane, M Rkain… - Cureus, 2024 - search.proquest.com
Sanjad-Sakati syndrome is an autosomal recessive disorder characterized by facial
dysmorphia, growth retardation, and congenital hypoparathyroidism. Epidemiologically, this …
dysmorphia, growth retardation, and congenital hypoparathyroidism. Epidemiologically, this …