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Am J Med Genet B Neuropsychiatr Genet ; 177(5): 520-528, 2018 07.
Artículo en Inglés | MEDLINE | ID: mdl-30134084

RESUMEN

Copy number variants at chromosome 17q12 have been associated with a spectrum of phenotypes. Deletions of 17q12 are well described and associated with maturity onset diabetes of the young type 5 (MODY5) and cystic renal disease (HNF1ß) as well as cognitive impairment and seizures. Duplication of 17q12 is emerging as a new genetic syndrome, associated with learning disability, seizures, and behavioral problems. The duplication is often inherited from an apparently unaffected parent. Here, we describe a three-generation family with multiple individuals carrying a17q12 microduplication with varying clinical features, consistent with variable penetrance. The proband who inherited a 1.8 Mb interstitial 17q12 duplication from his mother presented with developmental delay, behavioral problems, and mild dysmorphism. One of his sisters, his maternal uncle, and his maternal grandmother also carry the 17q12 microduplication. Clinical features of the carriers include renal problems, diabetes mellitus, learning difficulties, epilepsy and mental illness. Cognitive abilities range from normal function to moderate impairment (full-scale IQ range: 52-99). In light of recent reports of association of this locus with schizophrenia, we performed a detailed psychiatric assessment and confirmed that one family member has symptoms consistent with a diagnosis of schizophrenia and another has a prodromal syndrome with attenuated positive symptoms of psychosis. This report extends the clinical phenotype associated with the 17q12 microduplication and highlights the phenotypic variability.


Asunto(s)
Duplicación Cromosómica/genética , Cromosomas Humanos Par 17/genética , Anomalías Múltiples/genética , Adulto , Anciano , Niño , Preescolar , Deleción Cromosómica , Variaciones en el Número de Copia de ADN/genética , Discapacidades del Desarrollo/genética , Epilepsia/genética , Familia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Linaje , Fenotipo , Convulsiones/genética
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