Lachiewicz Sibley syndrome

Common Name(s)

Lachiewicz Sibley syndrome

Lachiewicz Sibley syndrome is a rare genetic disorder. This condition results from a mutation or error in a person’s DNA or genes. Symptoms of this disorder may include renal disease or preauricular sinus or cyst, which is a dent or dimple located next to the outer ear. Those with Lachiewicz Sibley syndrome may also have underdeveloped kidneys or excess protein in the urine. This condition is inherited as an autosomal dominant condition, which means that although there are two copies of each gene in almost every cell, only one of the copies has to have the changes or mutations to cause the symptoms. Many times this condition may run in families, and if one parent has the condition there is a 50% chance their child will have it too. Although there is currently no cure for Lachiewicz Sibley syndrome, there are various resources to help manage the condition and treat birth defects. Doctors seek help from various therapists and community services to provide support and care for families affected by Lachiewicz Sibley syndrome.

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Advocacy and Support Organizations

 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Lachiewicz Sibley syndrome" for support, advocacy or research.

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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 "Lachiewicz Sibley 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 "Lachiewicz Sibley 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.