Sanjad Sakati Syndrome: Case reports from Egypt

Sanjad Sakati Syndrome: Case reports from Egypt

Background: Sanjad Sakati Syndrome (SSS) is a rare autosomal recessive congenital disorder. It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth retardation, dysmorphic features, as well as mild to severe mental retardation. The prevalence of this syndrome is no...

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Bibliographic Details
Main Authors: Mona Hafez, Ghada M. Anwar, Amany Ibrahim, Noha Musa
Format: Article
Language:English
Published: SpringerOpen 2017-03-01
Series:Egyptian Pediatric Association Gazette
Subjects:
Sanjad-Sakati Syndrome
Hypoparathyroidism-retardation-dysmorphism
TBCE protein
Congenital hypoparathyroidism
Online Access:http://www.sciencedirect.com/science/article/pii/S1110663816300921

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http://www.sciencedirect.com/science/article/pii/S1110663816300921

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