Literature DB >> 23599697

Segmental Maternal UPD6 with Prenatal Growth Restriction.

G Poke1, M Doody, J Prado, M Gattas.   

Abstract

We report a child with segmental maternal uniparental isodisomy of chromosome 6, involving most of the long arm distal to 6q16, detected by SNP microarray. Clinical features include prenatal growth restriction, global developmental delay, and severe gastro-esophageal reflux disease. Maternal uniparental disomy (UPD) of chromosome 6 has previously been reported to cause intrauterine growth restriction. Paternal UPD of this chromosome is well known to cause transient neonatal diabetes mellitus. We discuss reported cases of maternal UPD of chromosome 6 and consider whether our patient's features may be due to disordered imprinting or unmasking of an autosomal recessive condition.

Entities:  

Keywords:  Failure to thrive; Intrauterine growth restriction; UPD6; Uniparental disomy

Year:  2012        PMID: 23599697      PMCID: PMC3569104          DOI: 10.1159/000345168

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  19 in total

1.  Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome.

Authors:  Elizabeth A Parker; Karine Hovanes; John Germak; Forbes Porter; Deborah P Merke
Journal:  Am J Med Genet A       Date:  2006-10-15       Impact factor: 2.802

2.  Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth.

Authors:  Annie Varrault; Charlotte Gueydan; Annie Delalbre; Anja Bellmann; Souheir Houssami; Cindy Aknin; Dany Severac; Laetitia Chotard; Malik Kahli; Anne Le Digarcher; Paul Pavlidis; Laurent Journot
Journal:  Dev Cell       Date:  2006-11       Impact factor: 12.270

Review 3.  Copy number and SNP arrays in clinical diagnostics.

Authors:  Christian P Schaaf; Joanna Wiszniewska; Arthur L Beaudet
Journal:  Annu Rev Genomics Hum Genet       Date:  2011       Impact factor: 8.929

4.  Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.

Authors:  Hakan Gümüş; Stijn Ghesquiere; Hüseyin Per; Meda Kondolot; Kimiyoshi Ichida; Gamze Poyrazoğlu; Sefer Kumandaş; John Engelen; Munis Dundar; Ahmet Okay Cağlayan
Journal:  Dev Med Child Neurol       Date:  2010-06-22       Impact factor: 5.449

5.  Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate.

Authors:  Iman Salahshourifar; Ahmad Sukari Halim; Wan Azman Wan Sulaiman; Bin Alwi Zilfalil
Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

6.  New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism.

Authors:  Eduardo Fernández-Rebollo; Beatriz Lecumberri; Intza Garin; Javier Arroyo; Ana Bernal-Chico; Fernando Goñi; Rosa Orduña; Luis Castaño; Guiomar Pérez de Nanclares
Journal:  Eur J Endocrinol       Date:  2010-09-13       Impact factor: 6.664

7.  Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome.

Authors:  K Sasaki; N Okamoto; K Kosaki; T Yorifuji; O Shimokawa; H Mishima; K-i Yoshiura; N Harada
Journal:  Clin Genet       Date:  2010-12-20       Impact factor: 4.438

8.  Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.

Authors:  T R Welch; L S Beischel; E Choi; K Balakrishnan; N A Bishof
Journal:  J Clin Invest       Date:  1990-08       Impact factor: 14.808

9.  A new genetic concept: uniparental disomy and its potential effect, isodisomy.

Authors:  E Engel
Journal:  Am J Med Genet       Date:  1980

Review 10.  Complex and segmental uniparental disomy updated.

Authors:  D Kotzot
Journal:  J Med Genet       Date:  2008-06-04       Impact factor: 6.318

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  6 in total

1.  Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.

Authors:  Jana Sachwitz; Getrud Strobl-Wildemann; György Fekete; Laima Ambrozaitytė; Vaidutis Kučinskas; Lukas Soellner; Matthias Begemann; Thomas Eggermann
Journal:  BMC Med Genet       Date:  2016-03-11       Impact factor: 2.103

2.  The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?

Authors:  Thomas Eggermann; Barbara Oehl-Jaschkowitz; Severin Dicks; Wolfgang Thomas; Deniz Kanber; Beate Albrecht; Matthias Begemann; Ingo Kurth; Jasmin Beygo; Karin Buiting
Journal:  Mol Genet Genomic Med       Date:  2017-09-22       Impact factor: 2.183

3.  Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction.

Authors:  Sandra Chantot-Bastaraud; Svea Stratmann; Frédéric Brioude; Matthias Begemann; Miriam Elbracht; Luitgard Graul-Neumann; Madeleine Harbison; Irène Netchine; Thomas Eggermann
Journal:  Mol Cytogenet       Date:  2017-07-25       Impact factor: 2.009

4.  Syndromic Disorders Caused by Disturbed Human Imprinting

Authors:  Diana Carli; Evelise Riberi; Giovanni Battista Ferrero; Alessandro Mussa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2019-04-10

5.  Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum.

Authors:  Tomoko Fuke; Akie Nakamura; Takanobu Inoue; Sayaka Kawashima; Kaori Isono Hara; Keiko Matsubara; Shinichiro Sano; Kazuki Yamazawa; Maki Fukami; Tsutomu Ogata; Masayo Kagami
Journal:  J Clin Endocrinol Metab       Date:  2021-03-08       Impact factor: 5.958

Review 6.  Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci.

Authors:  Thomas Eggermann; Guiomar Perez de Nanclares; Eamonn R Maher; I Karen Temple; Zeynep Tümer; David Monk; Deborah J G Mackay; Karen Grønskov; Andrea Riccio; Agnès Linglart; Irène Netchine
Journal:  Clin Epigenetics       Date:  2015-11-14       Impact factor: 6.551

  6 in total

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