The 20 Best Fanconi Bickel Syndrome Doctors in Mali

Find the Top Fanconi Bickel Syndrome Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 1 doctor with experience in Fanconi Bickel Syndrome near Mali. Of these, 1 are Experienced.

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1 provider found
    Experienced in Fanconi Bickel Syndrome

    Garan Dabo
    Experienced in Fanconi Bickel Syndrome

    Garan Dabo
    Bamako, BKO, ML 

    Garan Dabo practices practicing medicine in Bamako, Mali. Mr. Dabo is rated as an Experienced expert by MediFind in the treatment of Fanconi Bickel Syndrome. His clinical expertise encompasses Aminoaciduria, Fanconi Syndrome, Fanconi Bickel Syndrome, and HIV/AIDS.

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    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
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    Last Updated: 04/28/2026

    What is the definition of Fanconi Bickel Syndrome?

    Fanconi Bickel syndrome (FBS) is a rare condition characterized by the accumulation of a substance called glycogen in different parts of the body. Glycogen is created when the body needs to store glucose (sugar). When the body needs sugar again, glycogen is transformed back into glucose for use. People with Fanconi Bickel syndrome do not store the appropriate amount of glycogen. Therefore, Fanconi Bickel syndrome is known as a glycogen storage disease. Specifically, glycogen accumulates in the liver and kidneys. Signs and symptoms begin in the first few months of life and include growing slower than expected (failure to thrive), excessive urination (polyuria), and weakened bones (rickets). Later in life, children may have short stature and a swollen liver and spleen (hepatosplenomegaly). Fanconi Bickel syndrome is caused by genetic changes to the SLC2A2 gene and is inherited in an autosomal recessive manner. Diagnosis of FBS is based on a clinical examination that shows signs of FBS. The condition can be confirmed by genetic testing.