Literature DB >> 3631137

Urofacial (ochoa) syndrome.

B Ochoa, R J Gorlin.   

Abstract

Between 1965 and 1986 we saw 36 children with enuresis and urinary tract infection in association with "inversion" of facial expression when laughing. Urologic work-up of these patients disclosed characteristic findings of mild neuropathic bladder in all cases, with severe urinary tract damage in most of them. The clear association of distortion in facial expression and neuropathic bladder with resultant damage to the genitourinary tract should prompt urological evaluation of individuals with "inversion" of facial expression. About two thirds of the patients also had moderate to severe constipation. We suggest the term urofacial syndrome for this disorder. The occurrence of the disorder in multiple sibs, normal parents, increased parental consanguinity, and equal sex ratio indicate autosomal recessive inheritance.

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Year:  1987        PMID: 3631137     DOI: 10.1002/ajmg.1320270320

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


  19 in total

1.  Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24.

Authors:  C Y Wang; B Hawkins-Lee; B Ochoa; R D Walker; J X She
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

Review 2.  Dysfunctional voiding syndromes and vesicoureteral reflux.

Authors:  Y L Homsy
Journal:  Pediatr Nephrol       Date:  1994-02       Impact factor: 3.714

3.  Ochoa syndrome: a spectrum of urofacial syndrome.

Authors:  Ozgu Aydogdu; Berk Burgu; Fuat Demirel; Tarkan Soygur; Zeynep Birsin Ozcakar; Fatos Yalcinkaya; Serdar Tekgul
Journal:  Eur J Pediatr       Date:  2009-08-11       Impact factor: 3.183

4.  Mutations in HPSE2 cause urofacial syndrome.

Authors:  Sarah B Daly; Jill E Urquhart; Emma Hilton; Edward A McKenzie; Richard A Kammerer; Malcolm Lewis; Bronwyn Kerr; Helen Stuart; Dian Donnai; David A Long; Berk Burgu; Ozgu Aydogdu; Murat Derbent; Sixto Garcia-Minaur; Willie Reardon; Blanca Gener; Stavit Shalev; Rupert Smith; Adrian S Woolf; Graeme C Black; William G Newman
Journal:  Am J Hum Genet       Date:  2010-06-11       Impact factor: 11.025

5.  Loss-of-function mutations in HPSE2 cause the autosomal recessive urofacial syndrome.

Authors:  Junfeng Pang; Shu Zhang; Ping Yang; Bobbilynn Hawkins-Lee; Jixin Zhong; Yushan Zhang; Bernardo Ochoa; Jose A G Agundez; Marie-Antoinette Voelckel; Richard B Fisher; Weikuan Gu; Wen-Cheng Xiong; Lin Mei; Jin-Xiong She; Cong-Yi Wang
Journal:  Am J Hum Genet       Date:  2010-06-11       Impact factor: 11.025

6.  Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome.

Authors:  Wisam Al Badr; Suha Al Bader; Edgar Otto; Friedhelm Hildebrandt; Todd Ackley; Weiping Peng; Jishu Xu; Jun Li; Kailey M Owens; David Bloom; Jeffrey W Innis
Journal:  J Pediatr Urol       Date:  2011-03-29       Impact factor: 1.830

Review 7.  Contemporary and emerging drug treatments for urinary incontinence in children.

Authors:  Mitchell R Humphreys; Yuri E Reinberg
Journal:  Paediatr Drugs       Date:  2005       Impact factor: 3.022

Review 8.  Genetics of human congenital urinary bladder disease.

Authors:  Adrian S Woolf; Helen M Stuart; William G Newman
Journal:  Pediatr Nephrol       Date:  2013-04-13       Impact factor: 3.714

Review 9.  Clinical and genetic characteristics for the Urofacial Syndrome (UFS).

Authors:  Yaqin Tu; Ping Yang; Jia Yang; Yuchen Xu; Fei Xiong; Qilin Yu; Weikuan Gu; Dinel Pond; Nancy Mendelsohn; Guus A M A Lachmeijer; Shu Zhang; Cong-Yi Wang
Journal:  Int J Clin Exp Pathol       Date:  2014-04-15

10.  LRIG2 mutations cause urofacial syndrome.

Authors:  Helen M Stuart; Neil A Roberts; Berk Burgu; Sarah B Daly; Jill E Urquhart; Sanjeev Bhaskar; Jonathan E Dickerson; Murat Mermerkaya; Mesrur Selcuk Silay; Malcolm A Lewis; M Beatriz Orive Olondriz; Blanca Gener; Christian Beetz; Rita E Varga; Omer Gülpınar; Evren Süer; Tarkan Soygür; Zeynep B Ozçakar; Fatoş Yalçınkaya; Aslı Kavaz; Burcu Bulum; Adnan Gücük; Wyatt W Yue; Firat Erdogan; Andrew Berry; Neil A Hanley; Edward A McKenzie; Emma N Hilton; Adrian S Woolf; William G Newman
Journal:  Am J Hum Genet       Date:  2013-01-11       Impact factor: 11.025

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