Literature DB >> 14648341

Can a congenital dysfunctional bladder be diagnosed from a smile? The Ochoa syndrome updated.

Bernardo Ochoa1.   

Abstract

During the last 40 years over 100 patients have been reported with a dysfunctional lower urinary tract associated with a peculiar distortion of the facial expression. This most unusual disorder was initially considered a local observation. Time, however, has proven otherwise, since patients with this syndrome have now been reported from various countries throughout the world. This association of lower urinary tract and bowel dysfunction with an abnormal facial expression was named the urofacial (Ochoa) syndrome. Genetic studies have demonstrated that this condition is inherited as an autosomal recessive trait, and a potential gene has been mapped to chromosome 10q23-q24. There is also enough evidence to suggest that patients with this syndrome as well as those with subclinical neurological bladder, occult neuropathic bladder, non-neurogenic neurogenic bladder or Hinman syndrome, dysfunctional voiding, or dysfunctional elimination may be affected by the same congenital disorder of neurological origin.

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Year:  2003        PMID: 14648341     DOI: 10.1007/s00467-003-1291-1

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


  50 in total

1.  Surgical correction of bladder-neck obstruction in children.

Authors:  R E GROSS; J RANDOLPH; H M WISE
Journal:  N Engl J Med       Date:  1963-01-03       Impact factor: 91.245

2.  Vesical neck obstruction in children.

Authors:  M ANDREASSEN
Journal:  Acta Chir Scand       Date:  1953

Review 3.  The nonneurogenic neurogenic bladder of early infancy.

Authors:  V R Jayanthi; A E Khoury; G A McLorie; S K Agarwal
Journal:  J Urol       Date:  1997-09       Impact factor: 7.450

4.  Neurophysiological measurement of the voiding reflex arcs in patients with functional disorders of the lower urinary tract.

Authors:  A Fidas; R A Elton; A McInnes; G D Chisholm
Journal:  Br J Urol       Date:  1987-09

5.  The occult neuropathic bladder.

Authors:  D I Williams; G Hirst; D Doyle
Journal:  J Pediatr Surg       Date:  1974-02       Impact factor: 2.545

6.  Isolated neurogenic dysfunction of the bladder in children with urinary tract infection.

Authors:  B Kamhi; M I Horowitz; A Kovetz
Journal:  J Urol       Date:  1971-07       Impact factor: 7.450

7.  Face of the child as an index of disease.

Authors:  Y Paul
Journal:  Indian J Pediatr       Date:  1972-03       Impact factor: 1.967

Review 8.  Dysfunctional elimination syndrome in children without obvious spinal cord diseases.

Authors:  W C Feng; B M Churchill
Journal:  Pediatr Clin North Am       Date:  2001-12       Impact factor: 3.278

9.  Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French family.

Authors:  X Chauve; C Missirian; P Malzac; L Girardot; J M Guys; C Louis; N Philip; M A Voelckel
Journal:  Am J Med Genet       Date:  2000-11-06

Review 10.  Occult neuropathic bladder.

Authors:  L W Mix
Journal:  Urology       Date:  1977-07       Impact factor: 2.649

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  26 in total

1.  An adolescent boy progressing insidiously to end-stage renal disease: Answers.

Authors:  Aysun Çaltık Yılmaz; Bahar Buyukkaragoz; Selcuk Kivilcim; Aslı Celebi Tayfur; Sacit Gunbey
Journal:  Pediatr Nephrol       Date:  2017-06-19       Impact factor: 3.714

2.  Urinary tract effects of HPSE2 mutations.

Authors:  Helen M Stuart; Neil A Roberts; Emma N Hilton; Edward A McKenzie; Sarah B Daly; Kristen D Hadfield; Jeffery S Rahal; Natalie J Gardiner; Simon W Tanley; Malcolm A Lewis; Emily Sites; Brad Angle; Cláudia Alves; Teresa Lourenço; Márcia Rodrigues; Angelina Calado; Marta Amado; Nancy Guerreiro; Inês Serras; Christian Beetz; Rita-Eva Varga; Mesrur Selcuk Silay; John M Darlow; Mark G Dobson; David E Barton; Manuela Hunziker; Prem Puri; Sally A Feather; Judith A Goodship; Timothy H J Goodship; Heather J Lambert; Heather J Cordell; Anand Saggar; Maria Kinali; Christian Lorenz; Kristina Moeller; Franz Schaefer; Aysun K Bayazit; Stefanie Weber; William G Newman; Adrian S Woolf
Journal:  J Am Soc Nephrol       Date:  2014-08-21       Impact factor: 10.121

Review 3.  Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation.

Authors:  Adrian S Woolf; Helen M Stuart; Neil A Roberts; Edward A McKenzie; Emma N Hilton; William G Newman
Journal:  Pediatr Nephrol       Date:  2013-07-09       Impact factor: 3.714

4.  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

5.  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

6.  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

Review 7.  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 8.  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

9.  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

Review 10.  Lower urinary tract development and disease.

Authors:  Hila Milo Rasouly; Weining Lu
Journal:  Wiley Interdiscip Rev Syst Biol Med       Date:  2013-02-13
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