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"Minimal" holoprosencephaly in a 14q deletion syndrome patient.
Della Giustina, Elvio; Iodice, Alessandro; Spagnoli, Carlotta; Giovannini, Simona; Frattini, Daniele; Fusco, Carlo; Gobbi, Giuseppe; Zollino, Marcella; Neri, Giovanni.
Afiliação
  • Della Giustina E; Child Neurology Unit, IRCCS, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
  • Iodice A; Child Neurology Unit, IRCCS, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
  • Spagnoli C; Child Neurology Unit, IRCCS, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
  • Giovannini S; Child Neurology Unit, Bellaria Hospital, IRCCS Institute of Neurological Sciences, Bologna, Italy.
  • Frattini D; Child Neurology Unit, IRCCS, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
  • Fusco C; Child Neurology Unit, IRCCS, Santa Maria Nuova Hospital, Reggio Emilia, Italy.
  • Gobbi G; Child Neurology Unit, Bellaria Hospital, IRCCS Institute of Neurological Sciences, Bologna, Italy.
  • Zollino M; Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy.
  • Neri G; Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy.
Am J Med Genet A ; 173(12): 3216-3220, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29136354
We report on a patient with terminal deletion of the long arm of chromosome 14 displaying brain interhemispheric fusion limited to the midline anterior frontal cortex associated with hypoplastic corpus callosum and incomplete rotation of the left hippocampus in a clinical setting of motor and intellectual disability with poor language, and social behavior abnormalities with aggressiveness. Some possible correlations between clinical signs and symptoms and various aspects of the complex brain malformation are briefly discussed and compared with other known abnormalities of chromosome 14. The different neuropathology of the most common forms and the new forms of holoprosencephaly recently described is also discussed and leads us to suggest classifying the interhemispheric fusion of this case as a "minimal" form of holoprosencephaly. This appears to be the first description in a 14q deletion patient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 14 / Holoprosencefalia / Deleção Cromossômica Limite: Adult / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 14 / Holoprosencefalia / Deleção Cromossômica Limite: Adult / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália