Literature DB >> 25193386

Clinical and genetic characterization of a founder PKHD1 mutation in Afrikaners with ARPKD.

Lindsay Lambie1, Rasheda Amin, Fahmida Essop, Avital Cnaan, Amanda Krause, Lisa M Guay-Woodford.   

Abstract

BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) occurs in 1:20,000 live births. Disease expression is widely variable, with approximately 30 % of affected neonates dying perinatally, while others survive to adulthood. Mutations at the PKHD1 locus are responsible for all typical presentations. The objectives of this study were to define the clinical and genetic characteristics in a cohort of South African patients of Afrikaner origin, a population with a high prevalence of ARPKD.
METHODS: DNA from the cohort was analyzed for background haplotypes and the p.M627K mutation previously identified in two unrelated Afrikaner patients. The clinical phenotype of the homozygous group was characterized.
RESULTS: Analysis of 36 Afrikaner families revealed that 27 patients, from 24 (67 %) families, were homozygous for the p.M627K substitution, occurring on a common haplotype. The clinical phenotype of the homozygous individuals was variable.
CONCLUSIONS: Our data provide strong evidence that the p.M627K substitution is a founder mutation in the Afrikaner population and can be used for streamlined diagnostic testing for at-risk pregnancies. The observed clinical variability suggests that disease expression is modulated by other genetic loci or by gene-environment interactions.

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Year:  2014        PMID: 25193386     DOI: 10.1007/s00467-014-2917-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  25 in total

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Authors:  Lisa M Guay-Woodford; Christopher J Wright; Gerd Walz; Gary A Churchill
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2.  Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts.

Authors:  A M Sharp; L M Messiaen; G Page; C Antignac; M-C Gubler; L F Onuchic; S Somlo; G G Germino; L M Guay-Woodford
Journal:  J Med Genet       Date:  2005-04       Impact factor: 6.318

3.  PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats.

Authors:  Luiz F Onuchic; Laszlo Furu; Yasuyuki Nagasawa; Xiaoying Hou; Thomas Eggermann; Zhiyong Ren; Carsten Bergmann; Jan Senderek; Ernie Esquivel; Raoul Zeltner; Sabine Rudnik-Schöneborn; Michael Mrug; William Sweeney; Ellis D Avner; Klaus Zerres; Lisa M Guay-Woodford; Stefan Somlo; Gregory G Germino
Journal:  Am J Hum Genet       Date:  2002-03-15       Impact factor: 11.025

4.  Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway.

Authors:  Miguel A Garcia-Gonzalez; Luis F Menezes; Klaus B Piontek; Junya Kaimori; David L Huso; Terry Watnick; Luiz F Onuchic; Lisa M Guay-Woodford; Gregory G Germino
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5.  Autosomal recessive polycystic kidney disease: the clinical experience in North America.

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Journal:  Pediatrics       Date:  2003-05       Impact factor: 7.124

6.  Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen.

Authors:  K Zerres; G Mücher; L Bachner; G Deschennes; T Eggermann; H Kääriäinen; M Knapp; T Lennert; J Misselwitz; K E von Mühlendahl
Journal:  Nat Genet       Date:  1994-07       Impact factor: 38.330

7.  The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling.

Authors:  L M Guay-Woodford; G Muecher; S D Hopkins; E D Avner; G G Germino; A P Guillot; J Herrin; R Holleman; D A Irons; W Primack
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Review 8.  Measurement and estimation of GFR in children and adolescents.

Authors:  George J Schwartz; Dana F Work
Journal:  Clin J Am Soc Nephrol       Date:  2009-10-09       Impact factor: 8.237

9.  Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene.

Authors:  Luiz F Onuchic; Michal Mrug; Xiaoying Hou; Thomas Eggermann; Carsten Bergmann; Klaus Zerres; Ellis D Avner; Laszlo Furu; Stefan Somlo; Yasuyuki Nagasawa; Gregory G Germino; Lisa M Guay-Woodford
Journal:  Am J Med Genet       Date:  2002-07-15

10.  Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD).

Authors:  Magdalena Adeva; Mounif El-Youssef; Sandro Rossetti; Patrick S Kamath; Vickie Kubly; Mark B Consugar; Dawn M Milliner; Bernard F King; Vicente E Torres; Peter C Harris
Journal:  Medicine (Baltimore)       Date:  2006-01       Impact factor: 1.889

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  4 in total

1.  Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis.

Authors:  Salvatore Melchionda; Teresa Palladino; Stefano Castellana; Mario Giordano; Elisa Benetti; Patrizia De Bonis; Leopoldo Zelante; Luigi Bisceglia
Journal:  J Hum Genet       Date:  2016-05-26       Impact factor: 3.172

2.  The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan Awardees.

Authors:  Corinne Antignac; James P Calvet; Gregory G Germino; Jared J Grantham; Lisa M Guay-Woodford; Peter C Harris; Friedhelm Hildebrandt; Dorien J M Peters; Stefan Somlo; Vicente E Torres; Gerd Walz; Jing Zhou; Alan S L Yu
Journal:  J Am Soc Nephrol       Date:  2015-05-07       Impact factor: 10.121

3.  Genetic and Informatic Analyses Implicate Kif12 as a Candidate Gene within the Mpkd2 Locus That Modulates Renal Cystic Disease Severity in the Cys1cpk Mouse.

Authors:  Michal Mrug; Juling Zhou; Chaozhe Yang; Bruce J Aronow; Xiangqin Cui; Trenton R Schoeb; Gene P Siegal; Bradley K Yoder; Lisa M Guay-Woodford
Journal:  PLoS One       Date:  2015-08-21       Impact factor: 3.240

4.  Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman.

Authors:  Intisar Al Alawi; Elisa Molinari; Issa Al Salmi; Fatma Al Rahbi; Adhra Al Mawali; John A Sayer
Journal:  BMC Nephrol       Date:  2020-08-14       Impact factor: 2.388

  4 in total

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