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What is Fanconi-ichthyosis-dysmorphism?

What is Fanconi-ichthyosis-dysmorphism?

  • 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.

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

Fanconi-ichthyosis-dysmorphism: Introduction

Types of Fanconi-ichthyosis-dysmorphism:

Broader types of Fanconi-ichthyosis-dysmorphism:

How serious is Fanconi-ichthyosis-dysmorphism?

Complications of Fanconi-ichthyosis-dysmorphism: see complications of Fanconi-ichthyosis-dysmorphism

What causes Fanconi-ichthyosis-dysmorphism?

Causes of Fanconi-ichthyosis-dysmorphism: see causes of Fanconi-ichthyosis-dysmorphism

What are the symptoms of Fanconi-ichthyosis-dysmorphism?

Symptoms of Fanconi-ichthyosis-dysmorphism: see symptoms of Fanconi-ichthyosis-dysmorphism

Complications of Fanconi-ichthyosis-dysmorphism: see complications of Fanconi-ichthyosis-dysmorphism

Fanconi-ichthyosis-dysmorphism: Testing

Diagnostic testing: see tests for Fanconi-ichthyosis-dysmorphism.

Misdiagnosis: see misdiagnosis and Fanconi-ichthyosis-dysmorphism.

How is it treated?

Doctors and Medical Specialists for Fanconi-ichthyosis-dysmorphism: Neonatologist ; see also doctors and medical specialists for Fanconi-ichthyosis-dysmorphism.
Treatments for Fanconi-ichthyosis-dysmorphism: see treatments for Fanconi-ichthyosis-dysmorphism

Name and Aliases of Fanconi-ichthyosis-dysmorphism

Main name of condition: Fanconi-ichthyosis-dysmorphism

Other names or spellings for Fanconi-ichthyosis-dysmorphism:

Deal-Barratt-Dillon syndrome


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