Literature DB >> 22683912

Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophy.

L Kroeldrup1, S Kjaergaard, M Kirchhoff, K Kock, C Brasch-Andersen, M Kibaek, L B Ousager.   

Abstract

Muscular hypertrophy is a very rare finding on foetal ultrasonography. We present a case with recurrent muscular hypertrophy, liver enlargement and polyhydramnios in two pregnancies. One pregnancy was terminated due to suspicion of a storage disease, whereas the other led to delivery of a boy with muscular hypertrophy and mildly retarded psychomotor development. Array-CGH identified a small duplication of 7q36.3 including the Sonic Hedgehog (SHH) gene in both the aborted foetus and the live born male sib. Neither of the parents carried the 7q36.3 duplication. The consequences of overexpression of SHH in humans are not elucidated, but animal studies have suggested its importance in muscular hypertrophy. We suggest that the clinical findings in the presented case might be explained by the duplication and presumed overexpression of SHH.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22683912     DOI: 10.1016/j.ejmg.2012.04.009

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  7 in total

1.  Pure Distal 7q Duplication: Describing a Macrocephalic Neurodevelopmental Syndrome, Case Report and Review of the Literature.

Authors:  Kerri Bosfield; Jullianne Diaz; Eyby Leon
Journal:  Mol Syndromol       Date:  2021-03-29

2.  Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report.

Authors:  Bárbara Marques; Cristina Ferreira; Filomena Brito; Sónia Pedro; Cristina Alves; Teresa Lourenço; Marta Amorim; Hildeberto Correia
Journal:  Mol Cytogenet       Date:  2016-11-25       Impact factor: 2.009

3.  De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case report.

Authors:  Muna A Al Dhaibani; Diane Allingham-Hawkins; Ayman W El-Hattab
Journal:  BMC Med Genet       Date:  2017-10-23       Impact factor: 2.103

4.  Prenatal identification of two discontinuous maternally inherited chromosome 7q36.3 microduplications totaling 507 kb including the sonic hedgehog gene in a fetus with multiple congenital anomalies.

Authors:  Mark Micale; Bedford Embrey; Katie Hubbell; Kelly Beaudry-Rogers; Amy Whitten
Journal:  Clin Case Rep       Date:  2017-05-10

5.  The ADAMTS5 Metzincin Regulates Zebrafish Somite Differentiation.

Authors:  Carolyn M Dancevic; Yann Gibert; Joachim Berger; Adam D Smith; Clifford Liongue; Nicole Stupka; Alister C Ward; Daniel R McCulloch
Journal:  Int J Mol Sci       Date:  2018-03-07       Impact factor: 5.923

6.  Genome sequencing in families with congenital limb malformations.

Authors:  Jonas Elsner; Martin A Mensah; Stefan Mundlos; Malte Spielmann; Manuel Holtgrewe; Jakob Hertzberg; Stefania Bigoni; Andreas Busche; Marie Coutelier; Deepthi C de Silva; Nursel Elçioglu; Isabel Filges; Erica Gerkes; Katta M Girisha; Luitgard Graul-Neumann; Aleksander Jamsheer; Peter Krawitz; Ingo Kurth; Susanne Markus; Andre Megarbane; André Reis; Miriam S Reuter; Daniel Svoboda; Christopher Teller; Beyhan Tuysuz; Seval Türkmen; Meredith Wilson; Rixa Woitschach; Inga Vater; Almuth Caliebe; Wiebke Hülsemann; Denise Horn
Journal:  Hum Genet       Date:  2021-06-22       Impact factor: 4.132

7.  Cell-type specific features of circular RNA expression.

Authors:  Julia Salzman; Raymond E Chen; Mari N Olsen; Peter L Wang; Patrick O Brown
Journal:  PLoS Genet       Date:  2013-09-05       Impact factor: 5.917

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.