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Neurocase ; 27(3): 227-230, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-34010111

RESUMEN

Kleefstra syndrome (KS) is a genetic syndrome caused by a haploinsufficiency of the EHMT1 gene and characterized by intellectual disability, language disorders, childhood hypotonia and distinct facial features. Only a few cases of first episode of psychosis in KS have already been reported. We describe a young female patient with KS who presented a first episode of psychosis. In a context of an initial diagnosis wavering and a lack of recommendations, this clinical observation illustrates the importance of psychiatric comorbidities and their diagnostic and therapeutic complexity in KS; with a need for multidisciplinary management considering its specific aspects and vulnerabilities.


Asunto(s)
Anomalías Craneofaciales , Discapacidad Intelectual , Trastornos Psicóticos , Niño , Deleción Cromosómica , Cromosomas Humanos Par 9/genética , Anomalías Craneofaciales/complicaciones , Anomalías Craneofaciales/genética , Femenino , Cardiopatías Congénitas , N-Metiltransferasa de Histona-Lisina/genética , Humanos , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/genética , Trastornos Psicóticos/complicaciones , Trastornos Psicóticos/genética
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