Literature DB >> 1616282

An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study.

A Bideau1, G Brunet, E Heyer, H Plauchu, J M Robert.   

Abstract

An important concentration of patients with Rendu-Osler disease occurs in the Valserine valley of the French Jura. A study of marriages shows that, in spite of its somewhat remote location, the valley cannot be considered an isolate, but that, on the contrary, exogamy is widely practised. Only 17.8% of the genes of inhabitants during the present century can be traced to the original population, but persons affected with the disease belong to a subgroup of the population which has lived in the villages for more than 10 generations. All the patients in 85 sibships are related. The smallest number of originator couples who lived at the beginning of the eighteenth century amounts to 16, the unique originator may therefore have lived approximately four generations earlier. However, as other patients who lived at the periphery of the Valserine valley do not appear to be related to any patients living in the valley, and because there has been considerable immigration into the valley, a number of hypotheses to explain the distribution of the disease in the region remain possible.

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Year:  1992        PMID: 1616282     DOI: 10.1080/03014469200002112

Source DB:  PubMed          Journal:  Ann Hum Biol        ISSN: 0301-4460            Impact factor:   1.533


  14 in total

1.  Evidence of sex-linked effects on the inheritance of human longevity: a population-based study in the Valserine valley (French Jura), 18-20th centuries.

Authors:  A Cournil; J M Legay; F Schächter
Journal:  Proc Biol Sci       Date:  2000-05-22       Impact factor: 5.349

2.  Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia.

Authors:  F S Govani; A Giess; I G Mollet; M E Begbie; M D Jones; L Game; C L Shovlin
Journal:  Mol Syndromol       Date:  2013-04-11

3.  Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia.

Authors:  Claire L Shovlin; Ilenia Simeoni; Kate Downes; Zoe C Frazer; Karyn Megy; Maria E Bernabeu-Herrero; Abigail Shurr; Jennifer Brimley; Dilipkumar Patel; Loren Kell; Jonathan Stephens; Isobel G Turbin; Micheala A Aldred; Christopher J Penkett; Willem H Ouwehand; Luca Jovine; Ernest Turro
Journal:  Blood       Date:  2020-10-22       Impact factor: 22.113

4.  Gastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient.

Authors:  Minsu Ha; Yoon Jae Kim; Kwang An Kwon; Ki Baik Hahm; Mi-Jung Kim; Dong Kyu Kim; Young Jae Lee; S Paul Oh
Journal:  World J Gastroenterol       Date:  2012-04-21       Impact factor: 5.742

5.  Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life.

Authors:  A J Easey; G M F Wallace; J M B Hughes; J E Jackson; W J Taylor; C L Shovlin
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-06       Impact factor: 10.154

6.  Surgical Treatment vs Nonsurgical Treatment for Brain Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: A Retrospective Multicenter Consortium Study.

Authors:  Ali Tayebi Meybodi; Helen Kim; Jeffrey Nelson; Steven W Hetts; Timo Krings; Karel G terBrugge; Marie E Faughnan; Michael T Lawton
Journal:  Neurosurgery       Date:  2018-01-01       Impact factor: 4.654

Review 7.  Hereditary haemorrhagic telangiectasia: a clinical and scientific review.

Authors:  Fatima S Govani; Claire L Shovlin
Journal:  Eur J Hum Genet       Date:  2009-04-01       Impact factor: 4.246

8.  Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia.

Authors:  Bassam R Ali; Imen Ben-Rebeh; Anne John; Nadia A Akawi; Reham M Milhem; Nouf A Al-Shehhi; Mouza M Al-Ameri; Shamma A Al-Shamisi; Lihadh Al-Gazali
Journal:  PLoS One       Date:  2011-10-14       Impact factor: 3.240

9.  Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.

Authors:  Elisabetta Buscarini; Gioacchino Leandro; Dario Conte; Cesare Danesino; Erica Daina; Guido Manfredi; Guido Lupinacci; Gianfranco Brambilla; Fernanda Menozzi; Federico De Grazia; Pietro Gazzaniga; Giuseppe Inama; Roberto Bonardi; Pasquale Blotta; Pierangelo Forner; Carla Olivieri; Annalisa Perna; Maurizio Grosso; Giacomo Pongiglione; Edoardo Boccardi; Fabio Pagella; Giorgio Rossi; Alessandro Zambelli
Journal:  Dig Dis Sci       Date:  2011-02-03       Impact factor: 3.199

10.  Severity score for hereditary hemorrhagic telangiectasia.

Authors:  Giuseppe A Latino; Helen Kim; Jeffrey Nelson; Ludmila Pawlikowska; William Young; Marie E Faughnan
Journal:  Orphanet J Rare Dis       Date:  2014-12-29       Impact factor: 4.123

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