Literature DB >> 10756338

Three-year-old girl with partial trisomy 4p and partial monosomy 8p with resemblance to Brachmann-de Lange syndrome--another locus for Brachmann-de Lange syndrome on 4p?

U A Mau1, C Backsch, H Schaudt, F K Trefz, P Kaiser.   

Abstract

We describe a 3-year-old girl with partial trisomy 4p and partial monosomy 8p who had prenatal and postnatal growth retardation, mental retardation, no speech development, mild synophrys, hirsutism, apparently low-set ears, dysphonic hoarse voice, hyperactivity, and small hands with proximal placement of the thumbs. She had recurrent lung infections, due to earlier aspiration and immune deficiency (chronic granulomatous disease). Cytogenetic findings in this and other cases with suggestive phenotype may point to an additional locus for Brachmann-de Lange phenotype. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10756338     DOI: 10.1002/(sici)1096-8628(20000320)91:3<180::aid-ajmg4>3.0.co;2-r

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


  2 in total

1.  Familial Constitutional Rearrangement of Chromosomes 4 & 8: Phenotypically Normal Mother and Abnormal Progeny.

Authors:  Fulesh Kunwar; Sonal R Bakshi
Journal:  J Clin Diagn Res       Date:  2016-04-01

2.  Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.

Authors:  Viviane Neri de Souza Reis; João Paulo Kitajima; Ana Carolina Tahira; Ana Cecília Feio-Dos-Santos; Rodrigo Ambrósio Fock; Bianca Cristina Garcia Lisboa; Sérgio Nery Simões; Ana C V Krepischi; Carla Rosenberg; Naila Cristina Lourenço; Maria Rita Passos-Bueno; Helena Brentani
Journal:  PLoS One       Date:  2017-01-24       Impact factor: 3.240

  2 in total

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