Literature DB >> 22390114

More than meets the smile: facial muscle expression in children with Ochoa syndrome.

I Ganesan1, T Thomas.   

Abstract

The Ochoa syndrome is the association of a non-neurogenic neurogenic bladder with abnormal facial muscle expression. Patients are at risk for renal failure due to obstructive uropathy. We report a family of three siblings, with an emphasis on the abnormalities in facial expression. Careful examination shows an unusual co-contraction of the orbicularis oculi and orbicularis oris muscles only when full facial expressions are exhibited, across a range of emotional or voluntary situations. This suggests a peripheral disorder in facial muscle control. Two thirds of patients have anal sphincter abnormalities. Aberrant organisation of the facial motor and urinary-anal sphincter nuclei may explain these symptoms.

Entities:  

Mesh:

Year:  2011        PMID: 22390114

Source DB:  PubMed          Journal:  Med J Malaysia        ISSN: 0300-5283


  6 in total

1.  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 2.  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

Review 3.  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

4.  Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder.

Authors:  Neil A Roberts; Emma N Hilton; Filipa M Lopes; Subir Singh; Michael J Randles; Natalie J Gardiner; Karl Chopra; Riccardo Coletta; Zunera Bajwa; Robert J Hall; Wyatt W Yue; Franz Schaefer; Stefanie Weber; Roger Henriksson; Helen M Stuart; Håkan Hedman; William G Newman; Adrian S Woolf
Journal:  Kidney Int       Date:  2019-03-08       Impact factor: 10.612

5.  Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus.

Authors:  Neil A Roberts; Adrian S Woolf; Helen M Stuart; Raphaël Thuret; Edward A McKenzie; William G Newman; Emma N Hilton
Journal:  Hum Mol Genet       Date:  2014-04-01       Impact factor: 6.150

Review 6.  From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease.

Authors:  Neil A Roberts; Emma N Hilton; Adrian S Woolf
Journal:  Nephrol Dial Transplant       Date:  2015-08-27       Impact factor: 5.992

  6 in total

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