ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024
Hydrocephalus in Sanajd Sakati syndrome: a first clinical report.
Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Sanjad Sakati syndrome (SSS) is a rare autosomal recessive disorder seen among the Arab population and is characterized by congenital hypothyroidism, growth retardation, and dysmorphism. As a complication for that, the patient may present with several metabolic and septic complications. None of the patients in literature was described to have hydrocephalus. This case report aims at describing a case with SSS who presented to our center with hydrocephalus, which is to our knowledge the first case with this unusual presentation to be described in literature. In this report, we will also convey our experience in treating this complicated case and the way we dealt with the complications encountered during the hospital stay.
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