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Pineocytoma in a child with Pallister-Killian syndrome: a case report and review of the literature.
Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery 2024 April 31
Pallister-Killian syndrome (PKS; OMIM #601803) is a rare genetic disorder typically characterized by developmental delay, seizures, sparse temporal hair, and facial dysmorphisms. PKS is most frequently caused by mosaic supernumerary isochromosome 12p. Here, we report a 27-month-old girl with a prenatal diagnosis of PKS and a histopathological diagnosis of pineocytoma.
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