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Tucker Syndrome: Disease Bioinformatics

Tucker Syndrome is a rare condition that causes droopy eyelids and the paralysis of the vocal chords. Individuals with Tucker Syndrome may experience symptoms such as premature birth, droopy eyelids, weak leg or arm muscles, laryngeal abnormality and vocal cord paralysis. Because the condition is so rare, the cause of Tucker Syndrome is unknown. There is no cure for the condition, and treatment depends on the severity of the symptoms. If the vocal cord paralysis restricts the airflow of the individual, a tracheotomy or another form of surgery may be required. Voice and physical therapy is another treatment option for those with Tucker Syndrome.

Tucker Syndrome Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Tucker Syndrome below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 58 products for the study of Tucker Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.


Goat Polyclonal
Species Mouse
Applications WB, Block

1 Publication
Western Blot: PARN Antibody (4D12) [NBP2-46321] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY PARN.Immunohistochemistry: PARN Antibody (4D12) [NBP2-46321] - Analysis of Carcinoma of Human bladder tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)

Mouse monoclonal
Species Human
Applications WB, IHC

Related Genes

Tucker Syndrome has been researched against:

Related Pathways

Related Diseases

Tucker Syndrome has been studied in relation to diseases such as:

Related PTMs

Alternate Names

Tucker Syndrome is also known as Congenital Bilateral Recurrent Nerve Paralysis And Ptosis.