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Diseases » CCFDN » Introduction


CCFDN: Introduction

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.

Symptoms of CCFDN

Home Diagnostic Testing

Home medical testing related to CCFDN:

Wrongly Diagnosed with CCFDN?

CCFDN: Related Patient Stories

Causes of CCFDN

Read more about causes of CCFDN.

More information about causes of CCFDN:

Less Common Symptoms of CCFDN

CCFDN: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

CCFDN: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

CCFDN: Animations

Research about CCFDN

Visit our research pages for current research about CCFDN treatments.

Statistics for CCFDN

CCFDN: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about CCFDN, or answer someone else's question, on our message boards:

Definitions of CCFDN:

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


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