Fanconi syndrome is a disorder of the kidney tubes in which certain substances normally absorbed into the bloodstream by the kidneys are released into the urine instead.
Fanconi syndrome can be caused by faulty genes, or it may result later in life due to kidney damage. Sometimes the cause of Fanconi syndrome is unknown.
Common causes of Fanconi syndrome in children are genetic defects that affect the body's ability to break down certain compounds such as:
- Cystine (cystinosis)
- Fructose (fructose intolerance)
- Galactose (galactosemia)
- Glycogen (glycogen storage disease)
Cystinosis is the most common cause of Fanconi syndrome in children.
Other causes in children include:
- Exposure to heavy metals such as lead, mercury, or cadmium
- Lowe's disease, a rare genetic disorder of the eyes, brain, and kidneys
- Wilson's disease
In adults, Fanconi syndrome can be caused by various things that damage the kidneys, including:
- Passing large amounts of urine, which can lead to dehydration
- Bone pain
Exams and Tests
Laboratory tests may show that too much of the following substances may be lost in the urine:
Loss of these substances can lead to a variety of problems. Further tests and a physical exam may show signs of:
Many different diseases can cause Fanconi syndrome. The underlying cause and its symptoms should be treated as appropriate.
The prognosis depends on the underlying disease.
When to Contact a Medical Professional
Call your health care provider if you have dehydration or muscle weakness.
De Toni-Fanconi syndrome
Seifter JL. Potassium disorders. In: Goldman L, Ausiello D, eds.Cecil Medicine
Update Date 3/3/2014
Updated by: Charles Silberberg, DO, Private Practice specializing in Nephrology, Affiliated with New York Medical College, Division of Nephrology, Valhalla, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.