Literature DB >> 3377002

Optic nerve coloboma associated with renal disease.

R G Weaver1, L F Cashwell, W Lorentz, D Whiteman, K R Geisinger, M Ball.   

Abstract

Optic nerve colobomas can occur as sporadic abnormalities, may be inherited as an autosomal dominant defect, occur as part of syndromes, and are rarely associated with cardiac malformations and midline encephaloceles. Karcher [1979] described a father and son with the "morning glory" optic disc anomaly and renal disease as a new association. We report on two brothers with optic nerve colobomas associated with renal disease. The ophthalmologic findings and renal histopathology are presented. This second familial occurrence suggests that the association of optic nerve coloboma and renal disease is a newly recognized syndrome.

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Year:  1988        PMID: 3377002     DOI: 10.1002/ajmg.1320290318

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


  11 in total

1.  Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease.

Authors:  K Narahara; E Baker; S Ito; Y Yokoyama; S Yu; D Hewitt; G R Sutherland; M R Eccles; R I Richards
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  Colobomatous malformations of the eye.

Authors:  I H Maumenee; T N Mitchell
Journal:  Trans Am Ophthalmol Soc       Date:  1990

3.  A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease.

Authors:  Ken Saida; Koichi Kamei; Naoya Morisada; Masao Ogura; Kentaro Ogata; Kentaro Matsuoka; Kandai Nozu; Kazumoto Iijima; Shuichi Ito
Journal:  CEN Case Rep       Date:  2019-09-19

4.  Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations.

Authors:  L A Schimmenti; H E Cunliffe; L A McNoe; T A Ward; M C French; H H Shim; Y H Zhang; W Proesmans; A Leys; K A Byerly; S R Braddock; M Masuno; K Imaizumi; K Devriendt; M R Eccles
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 5.  Renal coloboma syndrome.

Authors:  Lisa A Schimmenti
Journal:  Eur J Hum Genet       Date:  2011-06-08       Impact factor: 4.246

6.  HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.

Authors:  Rosemary Thomas; Simone Sanna-Cherchi; Bradley A Warady; Susan L Furth; Frederick J Kaskel; Ali G Gharavi
Journal:  Pediatr Nephrol       Date:  2011-03-05       Impact factor: 3.714

7.  The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney.

Authors:  J Favor; R Sandulache; A Neuhäuser-Klaus; W Pretsch; B Chatterjee; E Senft; W Wurst; V Blanquet; P Grimes; R Spörle; K Schughart
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

8.  The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies.

Authors:  H E Cunliffe; L A McNoe; T A Ward; K Devriendt; H G Brunner; M R Eccles
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

9.  Congenital anomalies of kidney and hand: a review.

Authors:  Gopalakrishnan Natarajan; Dhanapriya Jeyachandran; Bala Subramaniyan; Dineshkumar Thanigachalam; Arul Rajagopalan
Journal:  Clin Kidney J       Date:  2013-02-03

10.  A new mutation in the PAX2 gene in a Papillorenal Syndrome patient.

Authors:  Rahul Rachwani Anil; Carlos Rocha-de-Lossada; Carlos Hernando Ayala; Manuela España Contreras
Journal:  Am J Ophthalmol Case Rep       Date:  2019-10-11
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