{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,14]],"date-time":"2026-07-14T15:31:16Z","timestamp":1784043076612,"version":"3.55.0"},"reference-count":19,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2006,6,2]],"date-time":"2006-06-02T00:00:00Z","timestamp":1149206400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Anesthesia"],"published-print":{"date-parts":[[2006,11]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Sanjad\u2013Sakati 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\u2010East countries. We report the anesthesia management of a 12\u2010year\u2010old boy with SSS for dental treatment, and discuss the anesthesia implications of this disorder.<\/jats:p>","DOI":"10.1111\/j.1460-9592.2006.01981.x","type":"journal-article","created":{"date-parts":[[2006,6,6]],"date-time":"2006-06-06T21:49:38Z","timestamp":1149630578000},"page":"1189-1192","source":"Crossref","is-referenced-by-count":8,"title":["Anesthesia management for the child with Sanjad\u2013Sakati syndrome"],"prefix":"10.1111","volume":"16","author":[{"given":"CARI M.","family":"PLATIS","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"DAVID","family":"WASERSPRUNG","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"LUDMYLA","family":"KACHKO","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"IGOR","family":"TSUNZER","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"JACOB","family":"KATZ","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2006,8,14]]},"reference":[{"key":"e_1_2_4_2_2","first-page":"271","article-title":"Congenital hypoparathyroidism with dysmorphic features: a new syndrome","volume":"23","author":"Sanjad SA","year":"1988","journal-title":"J Pediatr"},{"key":"e_1_2_4_3_2","doi-asserted-by":"publisher","DOI":"10.1136\/adc.66.2.193"},{"key":"e_1_2_4_4_2","first-page":"292","article-title":"The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay. 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