Literature DB >> 9382148

Dominant coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate.

D Ravine1, N K Ragge, D Stephens, M Oldridge, A O Wilkie.   

Abstract

Ocular colobomas and microphthalmos, isolated or as part of a syndrome, are usually sporadic and only rarely found in large families. A 4-generation family with autosomal dominant uveal coloboma and microphthalmos associated with cleft lip and palate was re-evaluated. Wide variability in expression is evident and more recently recognized manifestations include a complete spectrum of eye involvement, impairment of extraocular movement, mid-frequency sensorineural hearing loss, and hematuria. Learning difficulties requiring remedial teaching were present in one third of those affected and a neural tube defect has occurred in one presumed affected member. This family appears to present a unique phenotype, which provides an opportunity to identify a genetic locus involved in eye, ear, renal, primary palate, and brain development.

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Year:  1997        PMID: 9382148     DOI: 10.1002/(sici)1096-8628(19971017)72:2<227::aid-ajmg19>3.0.co;2-p

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


  8 in total

1.  Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation.

Authors:  N K Ragge; A Salt; J R O Collin; A Michalski; P A Farndon
Journal:  Br J Ophthalmol       Date:  2005-08       Impact factor: 4.638

Review 2.  Ocular coloboma: a reassessment in the age of molecular neuroscience.

Authors:  C Y Gregory-Evans; M J Williams; S Halford; K Gregory-Evans
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

3.  Long term maintenance of neural tube defects prevention in a high prevalence state.

Authors:  Julianne S Collins; Kristy K Atkinson; Jane H Dean; Robert G Best; Roger E Stevenson
Journal:  J Pediatr       Date:  2011-02-23       Impact factor: 4.406

4.  A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum.

Authors:  Angèle Tingaud-Sequeira; Aurélien Trimouille; Manju Salaria; Rachel Stapleton; Stéphane Claverol; Claudio Plaisant; Marc Bonneu; Estelle Lopez; Benoit Arveiler; Didier Lacombe; Caroline Rooryck
Journal:  Hum Genet       Date:  2021-01-21       Impact factor: 4.132

5.  National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.

Authors:  D Morrison; D FitzPatrick; I Hanson; K Williamson; V van Heyningen; B Fleck; I Jones; J Chalmers; H Campbell
Journal:  J Med Genet       Date:  2002-01       Impact factor: 6.318

6.  New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders.

Authors:  R Holt; F Ceroni; D A Bax; S Broadgate; D Gold Diaz; C Santos; D Gerrelli; N K Ragge
Journal:  Sci Rep       Date:  2017-08-11       Impact factor: 4.379

7.  Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.

Authors:  Kathleen A Williamson; Joe Rainger; James A B Floyd; Morad Ansari; Alison Meynert; Kishan V Aldridge; Jacqueline K Rainger; Carl A Anderson; Anthony T Moore; Matthew E Hurles; Angus Clarke; Veronica van Heyningen; Alain Verloes; Martin S Taylor; Andrew O M Wilkie; David R Fitzpatrick
Journal:  Am J Hum Genet       Date:  2014-01-23       Impact factor: 11.025

8.  Familial Optic Disc Pits in 2 Father-Son Pairs: Clinical Features and Genetic Analysis.

Authors:  Devin Betsch; Andrew Orr; Mathew Nightingale; Daniel Gaston; Rishi Gupta
Journal:  Case Rep Ophthalmol       Date:  2021-07-01
  8 in total

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