Genetic and Rare Diseases Information Center (GARD)


Other names people use for this condition
  • Persistence of mullerian derivatives, with lymphangiectasia and postaxial polydactyly
  • Urioste syndrome
  • Renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly

Urioste Martinez-Frias syndrome
Please note that the links contained on this search results page may take you to sites outside of the NIH. (See Disclaimer under Site Policies for details.)


These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.

If you have a question, please contact us — we will answer your question and update this page with new resources and information.



For more information about Urioste Martinez-Frias syndrome click on the boxes below:
Q&A More Detailed
Information
Support
Groups
NLM Gateway

Questions & Answers
If you would like to submit a question Contact GARD

   Click arrows to expand or collapse a Resource Section.
   Show All Resources   Hide All Resources




Note: If you need help accessing information in different file formats such as PDF, MP3, see Viewers, Players, and Plug-ins.