Pineocytoma in a child with Pallister-Killian syndrome: a case report and review of the literature.
Childs Nerv Syst
; 40(8): 2619-2623, 2024 Aug.
Article
em En
| MEDLINE
| ID: mdl-38689102
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.
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Texto completo:
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Coleções:
01-internacional
Base de dados:
MEDLINE
Limite:
Child, preschool
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Female
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Humans
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article