Literature DB >> 263435

Alkaptonuria in the Trencín District of Czechoslovakia.

S Srsen, F Cisárik, L Pásztor, L Harmecko.   

Abstract

For several years the Clinical Genetics Research Laboratory at Martin, Czechoslovakia, has been studying alkaptonuria (AU) in the northern part of the District of Trencín in Slovakia. These affected individuals are part of a group of 103 alkaptonurics originated mostly in the mountainous parts of Slovakia. We report results of pedigree analyses; population and affected-family biochemical urine screening; estimation of inbreeding coefficient, of exogamy rate and of average marital distance and of calculation of the frequency of the AU allele, and of homozygotes and heterozygotes in this portion of the Trencín District. Twelve homozygotes were found, but seven originated from a single hamlet in which a founder effect - genetic drift and inbreeding - are thought to account for the high prevalence of AU.

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Year:  1978        PMID: 263435     DOI: 10.1002/ajmg.1320020207

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Identification of forty cases with alkaptonuria in one village in Jordan.

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Journal:  Rheumatol Int       Date:  2011-11-16       Impact factor: 2.631

2.  Nine cases of Alkaptonuria in one family in southern Jordan.

Authors:  Mohammed Al-Sbou; Nesrin Mwafi
Journal:  Rheumatol Int       Date:  2010-12-03       Impact factor: 2.631

3.  Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse.

Authors:  S R Schmidt; A Gehrig; M R Koehler; M Schmid; C R Müller; W Kress
Journal:  Mamm Genome       Date:  1997-03       Impact factor: 2.957

4.  Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene.

Authors:  U Felbor; Y Mutsch; F Grehn; C R Müller; W Kress
Journal:  Br J Ophthalmol       Date:  1999-06       Impact factor: 4.638

5.  High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spots.

Authors:  A Zatková; D B de Bernabé; H Poláková; M Zvarík; E Feráková; V Bosák; V Ferák; L Kádasi; S R de Córdoba
Journal:  Am J Hum Genet       Date:  2000-10-02       Impact factor: 11.025

6.  Novel mutations in the homogentisate 1,2 dioxygenase gene identified in Jordanian patients with alkaptonuria.

Authors:  Mohammed Al-sbou
Journal:  Rheumatol Int       Date:  2011-03-25       Impact factor: 2.631

Review 7.  Garrod's Croonian Lectures (1908) and the charter 'Inborn Errors of Metabolism': albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008.

Authors:  Charles R Scriver
Journal:  J Inherit Metab Dis       Date:  2008-10-12       Impact factor: 4.982

8.  Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations.

Authors:  O Uyguner; E Goicoechea de Jorge; A Cefle; T Baykal; H Kayserili; K Cefle; M Demirkol; M Yuksel-Apak; S Rodriguez de Córdoba; B Wollnik
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 9.  A Mimic of Ankylosing Spondylitis, Ochronosis: Case Report and Review of the Literature.

Authors:  Philip Chu; Maria C Cuellar; Sonali J Bracken; Teresa K Tarrant
Journal:  Curr Allergy Asthma Rep       Date:  2021-03-05       Impact factor: 4.806

  9 in total

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