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...
Main Authors: | Mona Hafez, Ghada M. Anwar, Amany Ibrahim, Noha Musa |
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Format: | Article |
Language: | English |
Published: |
SpringerOpen
2017-03-01
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Series: | Egyptian Pediatric Association Gazette |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1110663816300921 |
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