Literature DB >> 9674899

Normal adaptive function with learning disability in duplication 8p including band p22.

S S Sklower Brooks1, M Genovese, H Gu, C J Duncan, A Shanske, E C Jenkins.   

Abstract

Duplication 8p usually results in a syndrome characterized by profound mental retardation, mild facial anomalies, and malformations of hand, heart, and brain. We report on a large kindred segregating a Y;8 translocation in whom several individuals have duplication 8p22-->8pter. These individuals have normal adaptive function despite their unbalanced karyotype. The family was studied with G-banding and fluorescent in situ hybridization (FISH) using probes to chromosomes 8 and Y. Comparison of this family with other reported cases defines a mild clinical outcome for trisomy 8p22-->8pter in contrast to the severe findings when the duplication involves a longer, more proximal segment.

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Year:  1998        PMID: 9674899     DOI: 10.1002/(sici)1096-8628(19980630)78:2<114::aid-ajmg3>3.3.co;2-6

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  A case of partial trisomy of chromosome 8p associated with autism.

Authors:  Katerina Papanikolaou; Elena Paliokosta; Jolanda Gyftodimou; Gerassimos Kolaitis; Sofia Vgenopoulou; Catherine Sarri; John Tsiantis
Journal:  J Autism Dev Disord       Date:  2006-07

2.  Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome.

Authors:  Gene S Fisch; Ryan Davis; Janey Youngblom; Jeff Gregg
Journal:  Behav Genet       Date:  2011-01-23       Impact factor: 2.805

Review 3.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

4.  Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.

Authors:  Mary Glancy; Angela Barnicoat; Rajan Vijeratnam; Sharon de Souza; Joanne Gilmore; Shuwen Huang; Viv K Maloney; N Simon Thomas; David J Bunyan; Ann Jackson; John C K Barber
Journal:  Eur J Hum Genet       Date:  2008-08-20       Impact factor: 4.246

5.  Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants.

Authors:  Harita Ghevaria; Roy Naja; Sioban SenGupta; Paul Serhal; Joy Delhanty
Journal:  Mol Cytogenet       Date:  2017-02-02       Impact factor: 2.009

6.  De novo 8p21.3→ p23.3 Duplication With t(4;8)(q35;p21.3) Translocation Associated With Mental Retardation, Autism Spectrum Disorder, and Congenital Heart Defects: Case Report With Literature Review.

Authors:  Cristina Gug; Dorina Stoicanescu; Ioana Mozos; Laura Nussbaum; Mariana Cevei; Danae Stambouli; Anca Gabriela Pavel; Gabriela Doros
Journal:  Front Pediatr       Date:  2020-07-08       Impact factor: 3.418

  6 in total

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