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

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

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Sanjad-Sakati syndrome (SSS; Online Mendelian Inheritance in Man [OMIM] #241410), also known as hypoparathyroidism-retardation-dysmorphism (HRD) syndrome, is an autosomal recessive disorder in which prenatal-onset extreme growth retardation, congenital hypoparathyroidism and craniofacial dysmorphism...

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Bibliographic Details
Main Authors: Agha S. Haider, Anuradha Ganesh, Adila Al-Kindi, Ahmad Al-Hinai, Nadia Al-Kharousi, Saif Al-Yaroubi, Sana Al-Zuhaibi
Format: Article
Language:English
Published: Sultan Qaboos University 2014-08-01
Series:Sultan Qaboos University Medical Journal
Subjects:
sanjad-sakati syndrome
tbce protein, human
corneal opacity, congenital
persistent fetal vasculature syndrome
nanophthalmos
hypoparathyroidism
case report
oman.
Online Access:https://journals.squ.edu.om/index.php/squmj/article/view/1942

Internet

https://journals.squ.edu.om/index.php/squmj/article/view/1942

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