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Fanconi-ichthyosis-dysmorphism: Introduction

Fanconi-ichthyosis-dysmorphism: A very rare syndrome characterized by scaly skin (ichthyosis), anemia, muscle anomalies and various other abnormalities. All six reported cases died within 6 months. More detailed information about the symptoms, causes, and treatments of Fanconi-ichthyosis-dysmorphism is available below.

Symptoms of Fanconi-ichthyosis-dysmorphism

Home Diagnostic Testing

Home medical testing related to Fanconi-ichthyosis-dysmorphism:

Wrongly Diagnosed with Fanconi-ichthyosis-dysmorphism?

Fanconi-ichthyosis-dysmorphism: Related Patient Stories

Fanconi-ichthyosis-dysmorphism: Complications

Review possible medical complications related to Fanconi-ichthyosis-dysmorphism:

Causes of Fanconi-ichthyosis-dysmorphism

Read more about causes of Fanconi-ichthyosis-dysmorphism.

Misdiagnosis and Fanconi-ichthyosis-dysmorphism

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to more »

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is that psoriasis is rare in children, and not often seen more »

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called "psoriatic arthritis". This arthritic more »

Fanconi-ichthyosis-dysmorphism: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Fanconi-ichthyosis-dysmorphism: Animations

Statistics for Fanconi-ichthyosis-dysmorphism

Fanconi-ichthyosis-dysmorphism: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Fanconi-ichthyosis-dysmorphism, or answer someone else's question, on our message boards:

Definitions of Fanconi-ichthyosis-dysmorphism:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Fanconi-ichthyosis-dysmorphism as a "rare disease".
Source - Orphanet


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