Literature DB >> 22887875

12q14 microdeletion syndrome and short stature with or without relative macrocephaly.

Toshiki Takenouchi1, Keisuke Enomoto, Toshihiko Nishida, Chiharu Torii, Tadaharu Okazaki, Takao Takahashi, Kenjiro Kosaki.   

Abstract

Patients with 12q14 microdeletion can present with short stature with or without relative macrocephaly. When associated with relative macrocephaly, the phenotype resembles Silver-Russell syndrome (SRS). Short stature is attributable to haploinsufficiency of HMGA2, but a patient with a deletion at the HMGA2 locus only did not have macrocephaly. Hence, the presence of a separate locus for a relative macrocephaly phenotype was suggested. Herein, we present a girl with a 12q14 microdeletion involving the HMGA2 locus who had short stature but did not have macrocephaly. Inclusion and exclusion mappings based on a quantitative review of the degree of relative macrocephaly and the extent of the deletions in previously reported patients with a 12q14 microdeletion demonstrated a presumptive interval for relative macrocephaly spanning a few megabases. These results confirm that a deletion spanning both HMGA2 and this presumptive interval locus would cause an SRS-like phenotype.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22887875     DOI: 10.1002/ajmg.a.35527

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

Authors:  Agostina De Crescenzo; Valentina Citro; Andrea Freschi; Angela Sparago; Orazio Palumbo; Maria Vittoria Cubellis; Massimo Carella; Pia Castelluccio; Maria Luigia Cavaliere; Flavia Cerrato; Andrea Riccio
Journal:  J Hum Genet       Date:  2015-03-26       Impact factor: 3.172

2.  12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature.

Authors:  Francesca Mercadante; Martina Busè; Emanuela Salzano; Tiziana Fragapane; Daniela Palazzo; Michela Malacarne; Maria Piccione
Journal:  Ital J Pediatr       Date:  2020-07-28       Impact factor: 2.638

3.  Hmga2 deficiency is associated with allometric growth retardation, infertility, and behavioral abnormalities in mice.

Authors:  Mi Ok Lee; Jingyi Li; Brian W Davis; Srijana Upadhyay; Hadil M Al Muhisen; Larry J Suva; Tracy M Clement; Leif Andersson
Journal:  G3 (Bethesda)       Date:  2022-02-04       Impact factor: 3.542

4.  12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region.

Authors:  Adrian Mc Cormack; Cynthia Sharpe; Nerine Gregersen; Warwick Smith; Ian Hayes; Alice M George; Donald R Love
Journal:  Case Rep Genet       Date:  2015-07-22

5.  12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?

Authors:  Sofia Dória; Daniela Alves; Maria João Pinho; Joel Pinto; Miguel Leão
Journal:  BMC Med Genomics       Date:  2020-01-03       Impact factor: 3.063

Review 6.  HMGA Genes and Proteins in Development and Evolution.

Authors:  Robert Vignali; Silvia Marracci
Journal:  Int J Mol Sci       Date:  2020-01-19       Impact factor: 5.923

  6 in total

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