Document Detail

Three new European cases of urofacial (Ochoa) syndrome.
MedLine Citation:
PMID:  11446407     Owner:  NLM     Status:  MEDLINE    
We report on three European cases of urofacial (Ochoa) syndrome. This entity was originally described in Colombian patients and very few cases have been reported from other countries. It is likely that they may be missed because of variability of the urinary problems and failure to recognize the characteristic facial grimacing. Establishing an early diagnosis has important consequences for the management and prognosis of urinary problems in these patients.
S Garcia-Minaur; F Oliver; J M Yanez; J R Soriano; F Quinn; W Reardon
Related Documents :
6276647 - Hypoglycemic peripheral neuropathy in association with insulinoma: implication of gluco...
6313467 - Widespread cytomegalovirus gastroenterocolitis in a patient with acquired immunodeficie...
24413637 - The effectiveness of physiotherapy for cervical dystonia: a systematic literature review.
19533787 - Poland syndrome with bilateral features: case description with review of the literature.
722437 - Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia).
22973317 - Cardiac epithelioid pecoma: report of two cases and review of the literature.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Clinical dysmorphology     Volume:  10     ISSN:  0962-8827     ISO Abbreviation:  Clin. Dysmorphol.     Publication Date:  2001 Jul 
Date Detail:
Created Date:  2001-07-11     Completed Date:  2001-12-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9207893     Medline TA:  Clin Dysmorphol     Country:  England    
Other Details:
Languages:  eng     Pagination:  165-70     Citation Subset:  IM    
Department of Paediatrics, Hospital de Cruces, Barakaldo, Spain.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Abnormalities, Multiple / pathology*
Facial Expression
Urinary Bladder, Neurogenic / pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Hirschsprung disease, mental retardation and dysmorphic facial features in five unrelated children.
Next Document:  Digitotalar dysmorphism with craniofacial and other new associated abnormalities.