Literature DB >> 1634233

Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p.

L Izquierdo1, M Porteous, P G Paramo, J M Connor.   

Abstract

Hereditary hydronephrosis (MIM 143400) is an autosomal dominant trait that causes unilateral or bilateral pelvi-ureteric junction (PUJ) obstruction. Linkage analysis was undertaken in 5 families with hereditary PUJ obstruction using the major histocompatibility complex locus as a test marker. The data as a whole supported a hereditary hydronephrosis locus on 6p. Maximal lod scores were 3.090 at a recombination fraction of 0.1 with full penetrance, and 2.486 at a recombination fraction of 0.1 with a penetrance of 90%. However, analysis of two point lod scores using the HOMOG program revealed significant evidence for genetic heterogeneity with one locus on 6p in 4 of the families, and a different locus in one family. After exclusion of this unlinked family, two point analysis gave a maximal lod score of 3.9 at a recombination fraction of 0.05 with full penetrance, and 4.2 at a recombination fraction of 0.0 with 90% penetrance. These data support the assignment of one of the loci for hereditary hydronephrosis to chromosome 6p.

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Year:  1992        PMID: 1634233     DOI: 10.1007/bf00219184

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  15 in total

Review 1.  Fetal uropathy.

Authors:  D F Thomas
Journal:  Br J Urol       Date:  1990-09

2.  Natural history of pelviureteric obstruction detected by prenatal sonography.

Authors:  A J Arnold; A M Rickwood
Journal:  Br J Urol       Date:  1990-01

3.  The postnatal management of hydronephrosis diagnosed by prenatal ultrasound.

Authors:  P G Ransley; H K Dhillon; I Gordon; P G Duffy; M J Dillon; T M Barratt
Journal:  J Urol       Date:  1990-08       Impact factor: 7.450

4.  The interrelationship between paraureteric diverticula, vesicoureteric reflux and duplication of the pelvicaliceal collecting system: a family study.

Authors:  J D Atwell; N H Allen
Journal:  Br J Urol       Date:  1980-08

5.  The coexistence of ureteropelvic junction obstruction and reflux.

Authors:  R L Lebowitz; J G Blickman
Journal:  AJR Am J Roentgenol       Date:  1983-02       Impact factor: 3.959

6.  Familial urinary tract anomalies: association with the major histocompatibility complex in man.

Authors:  D P Sengar; A Rashid; N M Wolfish
Journal:  J Urol       Date:  1979-02       Impact factor: 7.450

7.  Ureteropelvic junction obstruction and sibling uropathology.

Authors:  J Y Dwoskin
Journal:  Urology       Date:  1979-02       Impact factor: 2.649

8.  Pelviureteric obstruction in infancy and childhood. A review of 117 patients.

Authors:  D F Thomas; M Agrawal; A Z Laidin; H B Eckstein
Journal:  Br J Urol       Date:  1982-06

9.  Familial pelviureteric junction hydronephrosis and its association with a duplex pelvicaliceal system and vesicoureteric reflux. A family study.

Authors:  J D Atwell
Journal:  Br J Urol       Date:  1985-08

10.  Dominantly inherited ureteropelvic junction obstruction.

Authors:  M Buscemi; A Shanske; E Mallet; S Ozoktay; M K Hanna
Journal:  Urology       Date:  1985-12       Impact factor: 2.649

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  6 in total

1.  Pelvi-ureteric junction obstruction in autosomal-dominant polycystic kidney disease: an association yet to be reported.

Authors:  Neeraj Kumar Goyal; Apul Goel; Rahul Yadav; Satyanarayan Sankhwar
Journal:  BMJ Case Rep       Date:  2012-07-09

Review 2.  Genetic and developmental basis for urinary tract obstruction.

Authors:  Feng Chen
Journal:  Pediatr Nephrol       Date:  2008-12-16       Impact factor: 3.714

Review 3.  H-Y (SDM) antibody specifically binds Müllerian inhibiting substance.

Authors:  U Müller; S S Wachtel; V L Jaswaney; E H Goldberg
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

4.  Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

Authors:  S A Feather; S Malcolm; A S Woolf; V Wright; D Blaydon; C J Reid; F A Flinter; W Proesmans; K Devriendt; J Carter; P Warwicker; T H Goodship; J A Goodship
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

5.  Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.

Authors:  Shazia Ashraf; Bethan E Hoskins; Hassan Chaib; Julia Hoefele; Andreas Pasch; Pawaree Saisawat; Friedrich Trefz; Hans W Hacker; Gudrun Nuernberg; Peter Nuernberg; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Nephrol Dial Transplant       Date:  2009-12-10       Impact factor: 5.992

6.  A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.

Authors:  Maria Luisa Conte; Aida M Bertoli-Avella; Bianca M de Graaf; Francesca Punzo; Giuliana Lama; Angela La Manna; Carolina Grassia; Pier Francesco Rambaldi; Ben A Oostra; Silverio Perrotta
Journal:  Pediatr Nephrol       Date:  2008-01-16       Impact factor: 3.714

  6 in total

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