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,...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Hygeia Press di Corridori Marinella
2020-01-01
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| Series: | Journal of Pediatric and Neonatal Individualized Medicine |
| Subjects: | |
| Online Access: | https://www.jpnim.com/index.php/jpnim/article/view/765 |