Fine-Lubinsky Syndrome

Common Name(s)

Fine-Lubinsky Syndrome

Fine-Lubinsky syndrome is a very rare syndrome which has only been reported in a few individuals. Signs and symptoms may include brachycephaly (short or broad head), hearing loss, cataracts, intellectual disability, and several other features affecting various parts of the body. Although the majority of reported cases have been sporadic (occurring in individuals with no history of the disorder in the family), the syndrome has been reported in one pair of siblings with an apparently autosomal recessive inheritance pattern.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Fine-Lubinsky Syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Fine-Lubinsky Syndrome" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Fine-Lubinsky Syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.