Literature DB >> 19547944

[Language development impairment and trisomy 8 mosaicism].

M Ptok1, S Morlot.   

Abstract

Constitutional trisomy 8 mosaicism (46,XX/47,XX,+8 or 46,XY/47,XY,+8) is characterized by trisomic distribution of chromosomes in some but not all cells of the body. The full condition presents with physical stigmata, skeletal abnormalities and a mild to moderate cognitive impairment.Here we present a boy aged 3 years 10 months with partial trisomy 8 who was referred because of a language impairment. Because of known anomalies (corpus callous agenesis, deformities of the spine) a chromosomal analysis was initiated.This case highlights the necessity for an interdisciplinary diagnostic approach in children with language impairment and other constitutional disorders.

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Year:  2009        PMID: 19547944     DOI: 10.1007/s00106-008-1811-1

Source DB:  PubMed          Journal:  HNO        ISSN: 0017-6192            Impact factor:   1.284


  20 in total

1.  Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.

Authors:  C Danesino; F Pasquali; C Dellavecchia; E Maserati; A Minelli; L Seghezzi
Journal:  Am J Med Genet       Date:  1998-12-28

2.  [Trisomy 8 mosaicism syndrome].

Authors:  P Hummel; G Krohn-Jaster
Journal:  Z Kinder Jugendpsychiatr       Date:  1988-12

Review 3.  Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases.

Authors:  Emanuela Maserati; Fiorenza Aprili; Fabrizio Vinante; Franco Locatelli; Giovanni Amendola; Adriana Zatterale; Giuseppe Milone; Antonella Minelli; Franca Bernardi; Francesco Lo Curto; Francesco Pasquali
Journal:  Genes Chromosomes Cancer       Date:  2002-01       Impact factor: 5.006

Review 4.  Corpus callosum and simple visuomotor integration.

Authors:  G Berlucchi; S Aglioti; C A Marzi; G Tassinari
Journal:  Neuropsychologia       Date:  1995-08       Impact factor: 3.139

5.  Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicism.

Authors:  A F Brady; C S Waters; M J Pocha; L A Brueton
Journal:  Clin Genet       Date:  2000-08       Impact factor: 4.438

6.  Absence of disconnexion syndrome in callosal agenesis and early callosotomy: brain reorganization or lack of structural specificity during ontogeny?

Authors:  M Lassonde; H Sauerwein; A J Chicoine; G Geoffroy
Journal:  Neuropsychologia       Date:  1991       Impact factor: 3.139

Review 7.  Cognitive and sensori-motor functioning in the absence of the corpus callosum: neuropsychological studies in callosal agenesis and callosotomized patients.

Authors:  H C Sauerwein; M Lassonde
Journal:  Behav Brain Res       Date:  1994-10-20       Impact factor: 3.332

8.  Interhemispheric integration of simple visuomotor responses in patients with partial callosal defects.

Authors:  G Tassinari; S Aglioti; R Pallini; G Berlucchi; G F Rossi
Journal:  Behav Brain Res       Date:  1994-10-20       Impact factor: 3.332

Review 9.  Agenesis of the corpus callosum: clinical, neuroradiological and cytogenetic studies.

Authors:  D Serur; J S Jeret; K Wisniewski
Journal:  Neuropediatrics       Date:  1988-05       Impact factor: 1.947

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  1 in total

1.  [Tetrasomy 18p syndrome and hearing loss. An unusual case].

Authors:  C Schwemmle; M Arslan-Kirchner; B Pabst; M Ptok
Journal:  HNO       Date:  2012-10       Impact factor: 1.284

  1 in total

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