Literature DB >> 17935233

Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growth.

Cedric Le Caignec1, Bertrand Isidor, Ulrika de Pontbriand, Valerie David, Marie-Pierre Audrezet, Claude Ferec, Albert David.   

Abstract

Many patients with maternal uniparental disomy of chromosome 7 (UPD7) have been described, mainly with intrauterine and postnatal growth retardation or with Silver-Russell syndrome. In contrast, only three cases of paternal UPD7 have been reported, all associated with recessive disorders. Here, we report on the clinical and molecular data of the third patient with paternal UPD7 and cystic fibrosis. Pre- and postnatal growth were normal. These findings support the hypothesis that paternal isodisomy for human chromosome 7 may have no phenotypic effect on growth. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17935233     DOI: 10.1002/ajmg.a.31999

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


  10 in total

1.  Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.

Authors:  Els Dequeker; Manfred Stuhrmann; Michael A Morris; Teresa Casals; Carlo Castellani; Mireille Claustres; Harry Cuppens; Marie des Georges; Claude Ferec; Milan Macek; Pier-Franco Pignatti; Hans Scheffer; Marianne Schwartz; Michal Witt; Martin Schwarz; Emmanuelle Girodon
Journal:  Eur J Hum Genet       Date:  2008-08-06       Impact factor: 4.246

2.  Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.

Authors:  Jennifer M Kalish; Laura K Conlin; Tricia R Bhatti; Holly A Dubbs; Mary Catherine Harris; Kosuke Izumi; Sogol Mostoufi-Moab; Surabhi Mulchandani; Sulagna Saitta; Lisa J States; Daniel T Swarr; Alisha B Wilkens; Elaine H Zackai; Kristin Zelley; Marisa S Bartolomei; Kim E Nichols; Andrew A Palladino; Nancy B Spinner; Matthew A Deardorff
Journal:  Am J Med Genet A       Date:  2013-06-26       Impact factor: 2.802

3.  Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report.

Authors:  Cristina Bulli; Pier Antonio Battistella; Marta Bordignon; Placido Bramanti; Giuseppe Novelli; Federica Sangiuolo
Journal:  Cases J       Date:  2009-04-29

Review 4.  New developments in Silver-Russell syndrome and implications for clinical practice.

Authors:  Miho Ishida
Journal:  Epigenomics       Date:  2016-04-12       Impact factor: 4.778

5.  Homozygous Deletion of the CFTR Gene Caused by Interstitial Maternal Isodisomy in a Peruvian Child with Cystic Fibrosis.

Authors:  Flor Vásquez Sotomayor; Hugo Hernán Abarca-Barriga
Journal:  J Pediatr Genet       Date:  2019-02-13

Review 6.  Maternal uniparental isodisomy causing autosomal recessive GM1 gangliosidosis: a clinical report.

Authors:  Jessica E King; Amy Dexter; Inder Gadi; Val Zvereff; Meaghan Martin; Miriam Bloom; Adeline Vanderver; Amy Pizzino; Johanna L Schmidt
Journal:  J Genet Couns       Date:  2014-04-30       Impact factor: 2.537

7.  Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children.

Authors:  Mari Muurinen; Katariina Hannula-Jouppi; Lovisa E Reinius; Cilla Söderhäll; Simon Kebede Merid; Anna Bergström; Erik Melén; Göran Pershagen; Marita Lipsanen-Nyman; Dario Greco; Juha Kere
Journal:  Sci Rep       Date:  2017-11-16       Impact factor: 4.379

8.  Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum features.

Authors:  Siren Berland; Cecilie F Rustad; Mariann H L Bentsen; Embjørg J Wollen; Gitta Turowski; Stefan Johansson; Gunnar Houge; Bjørn I Haukanes
Journal:  Cold Spring Harb Mol Case Stud       Date:  2021-12-09

9.  Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.

Authors:  Katariina Hannula-Jouppi; Mari Muurinen; Marita Lipsanen-Nyman; Lovisa E Reinius; Sini Ezer; Dario Greco; Juha Kere
Journal:  Epigenetics       Date:  2013-11-18       Impact factor: 4.528

10.  Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype.

Authors:  Niu Li; Y U Ding; Tingting Yu; Juan Li; Yongnian Shen; Xiumin Wang; Qihua Fu; Yiping Shen; Xiaodong Huang; Jian Wang
Journal:  Exp Ther Med       Date:  2016-04-11       Impact factor: 2.447

  10 in total

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