Literature DB >> 11045594

Overlap between Baller-Gerold and Rothmund-Thomson syndrome.

A Mégarbané, I Melki, N Souraty, J Gerbaka, V El Ghouzzi, J Bonaventure, A Mornand, J Loiselet.   

Abstract

We report a male patient with craniosysnostosis, bilateral radial and ulnar hypoplasia, absent thumbs, poikiloderma, and short stature. His parents are first cousins. Although this patient was originally diagnosed as having Baller-Gerold syndrome it is more likely that he has Rothmund-Thomson syndrome or a similar disorder. This report confirms the overlap between these two syndromes, and that Baller-Gerold syndrome is essentially a diagnosis of exclusion.

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Year:  2000        PMID: 11045594     DOI: 10.1097/00019605-200009040-00018

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  10 in total

1.  Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

Authors:  Roberto Mendoza-Londono; Edward Lammer; Rosemarie Watson; John Harper; Atsushi Hatamochi; Saori Hatamochi-Hayashi; Dobrawa Napierala; Pia Hermanns; Sinead Collins; Benjamin B Roa; Madhuri R Hedge; Keiko Wakui; Diep Nguyen; David W Stockton; Brendan Lee
Journal:  Am J Hum Genet       Date:  2005-05-27       Impact factor: 11.025

2.  Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene.

Authors:  L Van Maldergem; H A Siitonen; N Jalkh; E Chouery; M De Roy; V Delague; M Muenke; E W Jabs; J Cai; L L Wang; S E Plon; C Fourneau; M Kestilä; Y Gillerot; A Mégarbané; A Verloes
Journal:  J Med Genet       Date:  2005-06-17       Impact factor: 6.318

3.  Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes.

Authors:  Yves Sznajer; H Annika Siitonen; Gaia Roversi; Chantal Dangoisse; Michèle Scaillon; France Ziereisen; Sylvie Tenoutasse; Marjo Kestilä; Lidia Larizza
Journal:  Eur J Pediatr       Date:  2007-03-20       Impact factor: 3.183

Review 4.  Rothmund-Thomson syndrome.

Authors:  Lidia Larizza; Gaia Roversi; Ludovica Volpi
Journal:  Orphanet J Rare Dis       Date:  2010-01-29       Impact factor: 4.123

5.  The mutation spectrum in RECQL4 diseases.

Authors:  H Annika Siitonen; Jenni Sotkasiira; Martine Biervliet; Abdelmadjid Benmansour; Yline Capri; Valerie Cormier-Daire; Barbara Crandall; Katariina Hannula-Jouppi; Raoul Hennekam; Denise Herzog; Kathelijn Keymolen; Marita Lipsanen-Nyman; Peter Miny; Sharon E Plon; Stefan Riedl; Ajoy Sarkar; Fernando R Vargas; Alain Verloes; Lisa L Wang; Helena Kääriäinen; Marjo Kestilä
Journal:  Eur J Hum Genet       Date:  2008-08-20       Impact factor: 4.246

6.  Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations.

Authors:  Elisa Adele Colombo; Hatice Mutlu-Albayrak; Yousef Shafeghati; Mine Balasar; Juliette Piard; Davide Gentilini; Anna Maria Di Blasio; Cristina Gervasini; Lionel Van Maldergem; Lidia Larizza
Journal:  Front Pediatr       Date:  2019-05-28       Impact factor: 3.418

Review 7.  Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies.

Authors:  Chiara Parodi; Elisabetta Di Fede; Angela Peron; Ilaria Viganò; Paolo Grazioli; Silvia Castiglioni; Richard H Finnell; Cristina Gervasini; Aglaia Vignoli; Valentina Massa
Journal:  Front Cell Dev Biol       Date:  2021-04-20

Review 8.  Molecular Mechanisms of the RECQ4 Pathogenic Mutations.

Authors:  Xiaohua Xu; Chou-Wei Chang; Min Li; Chao Liu; Yilun Liu
Journal:  Front Mol Biosci       Date:  2021-11-18

Review 9.  DNA Repair Syndromes and Cancer: Insights Into Genetics and Phenotype Patterns.

Authors:  Richa Sharma; Sara Lewis; Marcin W Wlodarski
Journal:  Front Pediatr       Date:  2020-10-23       Impact factor: 3.418

Review 10.  Role and Regulation of the RECQL4 Family during Genomic Integrity Maintenance.

Authors:  Thong T Luong; Kara A Bernstein
Journal:  Genes (Basel)       Date:  2021-11-29       Impact factor: 4.096

  10 in total

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