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Paediatric anaesthesia · Nov 2006
Case ReportsAnesthesia management for the child with Sanjad-Sakati syndrome.
- Cari M Platis, David Wasersprung, Ludmyla Kachko, Igor Tsunzer, and Jacob Katz.
- Department of Anesthesia, Schneider Children's Medical Center of Israel, Tel Aviv, Israel. carip@clalit.org.il
- Paediatr Anaesth. 2006 Nov 1; 16 (11): 1189-92.
AbstractSanjad-Sakati syndrome (SSS) is a rare genetic disorder characterized by congenital hypoparathyroidism, hypocalcemia and hyperphosphatemia, seizures, severe intrauterine and postnatal growth failure, dwarfism, mental retardation, dysmorphic features including retromicrognathia and abnormal dentition and increased susceptibility to infection. It is mainly confined to children in the Middle-East countries. We report the anesthesia management of a 12-year-old boy with SSS for dental treatment, and discuss the anesthesia implications of this disorder.
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