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Pineocytoma in a child with Pallister-Killian syndrome: a case report and review of the literature.
- Source :
-
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2024 Aug; Vol. 40 (8), pp. 2619-2623. Date of Electronic Publication: 2024 Apr 30. - Publication Year :
- 2024
-
Abstract
- 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.<br /> (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Details
- Language :
- English
- ISSN :
- 1433-0350
- Volume :
- 40
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
- Publication Type :
- Academic Journal
- Accession number :
- 38689102
- Full Text :
- https://doi.org/10.1007/s00381-024-06426-4