Assessment
Questionnaire
See what questions
a doctor would ask.
CCFDN: A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy. More detailed information about the symptoms, causes, and treatments of CCFDN is available below.
See full list of 18 symptoms of CCFDN
Home medical testing related to CCFDN:
Read more about causes of CCFDN.
More information about causes of CCFDN:
Read more about symptoms of CCFDN
Commonly undiagnosed diseases in related medical categories:
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
More CCFDN animations & videos
Visit our research pages for current research about CCFDN treatments.
Types of CCFDN
Read about other experiences, ask a question about CCFDN, or answer someone else's question, on our message boards:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list CCFDN as a "rare disease".
Source - Orphanet
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2011 Health Grades Inc. All rights reserved. Last Update: 7 May, 2013 (4:34)