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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Format: | Article |
Language: | English |
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Hygeia Press di Corridori Marinella
2020-01-01
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Series: | Journal of Pediatric and Neonatal Individualized Medicine |
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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. |
first_indexed | 2024-12-13T12:41:21Z |
format | Article |
id | doaj.art-57718e0fe90c471d961dbb6f3218e3df |
institution | Directory Open Access Journal |
issn | 2281-0692 |
language | English |
last_indexed | 2024-12-13T12:41:21Z |
publishDate | 2020-01-01 |
publisher | Hygeia Press di Corridori Marinella |
record_format | Article |
series | Journal of Pediatric and Neonatal Individualized Medicine |
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 |
work_keys_str_mv | AT allamfayezabuhamda sanjadsakatisyndromewithcornealopacityinapalestinianneonatecasereport AT aymenmohammedelsous sanjadsakatisyndromewithcornealopacityinapalestinianneonatecasereport |