Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report

Sanjad-Sakati syndrome is an autosomal recessive disorder found mainly in people of Arabian origin. This is a report of a Palestinian premature (35 weeks gestation) newborn who was part of twins and had this rare disease. The syndrome comprises congenital hypoparathyroidism, hypocalcaemia, seizure,...

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Main Authors: Allam Fayez Abuhamda, Aymen Mohammed Elsous
Format: Article
Language:English
Published: Hygeia Press di Corridori Marinella 2020-01-01
Series:Journal of Pediatric and Neonatal Individualized Medicine
Subjects:
Online Access:https://www.jpnim.com/index.php/jpnim/article/view/765
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author Allam Fayez Abuhamda
Aymen Mohammed Elsous
author_facet Allam Fayez Abuhamda
Aymen Mohammed Elsous
author_sort Allam Fayez Abuhamda
collection DOAJ
description Sanjad-Sakati syndrome is an autosomal recessive disorder found mainly in people of Arabian origin. This is a report of a Palestinian premature (35 weeks gestation) newborn who was part of twins and had this rare disease. The syndrome comprises congenital hypoparathyroidism, hypocalcaemia, seizure, severe growth retardation, low IQ and typical facial features. In addition, the baby had corneal opacity, although his elder brother with the same syndrome had not. Supportive treatment in the form of oral vitamin D and calcium are often offered to these children to treat hypocalcaemia.
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spelling doaj.art-57718e0fe90c471d961dbb6f3218e3df2022-12-21T23:45:38ZengHygeia Press di Corridori MarinellaJournal of Pediatric and Neonatal Individualized Medicine2281-06922020-01-0191e090123e09012310.7363/090123643Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case reportAllam Fayez Abuhamda0Aymen Mohammed Elsous1NICU Department, Shifa Hospital, Gaza Strip, PalestineFaculty of Health Professions, Israa University, Gaza Strip, Palestine; Unit of Planning and Policy Formulation, Ministry of Health, Gaza Strip, PalestineSanjad-Sakati syndrome is an autosomal recessive disorder found mainly in people of Arabian origin. This is a report of a Palestinian premature (35 weeks gestation) newborn who was part of twins and had this rare disease. The syndrome comprises congenital hypoparathyroidism, hypocalcaemia, seizure, severe growth retardation, low IQ and typical facial features. In addition, the baby had corneal opacity, although his elder brother with the same syndrome had not. Supportive treatment in the form of oral vitamin D and calcium are often offered to these children to treat hypocalcaemia.https://www.jpnim.com/index.php/jpnim/article/view/765sanjad-sakati syndromecorneal opacitypalestinian premature newbornhypoparathyroidism
spellingShingle Allam Fayez Abuhamda
Aymen Mohammed Elsous
Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
Journal of Pediatric and Neonatal Individualized Medicine
sanjad-sakati syndrome
corneal opacity
palestinian premature newborn
hypoparathyroidism
title Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
title_full Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
title_fullStr Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
title_full_unstemmed Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
title_short Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
title_sort sanjad sakati syndrome with corneal opacity in a palestinian neonate case report
topic sanjad-sakati syndrome
corneal opacity
palestinian premature newborn
hypoparathyroidism
url https://www.jpnim.com/index.php/jpnim/article/view/765
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