Literature DB >> 11477611

Maternal isochromosome 7q and paternal isochromosome 7p in a boy with growth retardation.

D Kotzot1, H Holland, E Keller, U G Froster.   

Abstract

A 12-year 9-month-old boy with postnatal growth retardation, normal psychomotor development, and minor anomalies that included a triangular-shaped face, small nose, and narrow and high-arched palate is reported. The constitutional karyotype was 46,XY,i(7)(p10),i(7)(q10). Molecular investigations revealed the presence of a maternal isodisomy 7q and a paternal isodisomy 7p. The clinical and molecular findings are notably congruent with a recently reported case and support the hypothesis of one or more maternally imprinted genes located on the long arm of chromosomes 7 that regulate, in particular, postnatal growth. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11477611     DOI: 10.1002/ajmg.1430

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


  2 in total

1.  An Infertile Man with Complementary Isochromosome of 46, XY, I(5)(P10),I(5)(Q10): A Case Report.

Authors:  Yu He; Bo Liu; Hui-Ling Wu; Shan Huang; Yun-Wei Qi; Hui-Han Zhao; Xue Qin; Shan Li
Journal:  Iran J Public Health       Date:  2019-09       Impact factor: 1.429

2.  Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum features.

Authors:  Siren Berland; Cecilie F Rustad; Mariann H L Bentsen; Embjørg J Wollen; Gitta Turowski; Stefan Johansson; Gunnar Houge; Bjørn I Haukanes
Journal:  Cold Spring Harb Mol Case Stud       Date:  2021-12-09
  2 in total

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