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

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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Autors principals: Haider, Agha S., Ganesh, Anuradha, Al-Kindi, Adila, Al-Hinai, Ahmad, Al-Kharousi, Nadia, Al-Yaroubi, Saif, Al-Zuhaibi, Sana
Format: Artigo
Idioma:Inglês
Publicat: Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences 2014
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4117669/
https://ncbi.nlm.nih.gov/pubmed/25097779
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