Fanconi syndrome
De Toni-Fanconi-Debré syndrome
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.
Causes
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 variations 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 syndrome, a rare genetic disorder of the eyes, brain, and kidneys
- Wilson disease
- Dent disease, a rare genetic disorder of the kidneys
In adults, Fanconi syndrome can be caused by various things that damage the kidneys, including:
- Certain medicines, including azathioprine, cidofovir, gentamicin, and tetracycline
- Kidney transplant
- Light chain deposition disease
- Multiple myeloma
- Primary amyloidosis
Symptoms
Symptoms include:
- Passing large amounts of urine, which can lead to dehydration
- Excessive thirst
- Severe bone pain
- Fractures due to bone weakness
- Muscle weakness
Exams and Tests
Laboratory tests may show that too much of the following substances may be lost in the urine:
- Amino acids
- Bicarbonate
- Glucose
- Magnesium
- Phosphate
- Potassium
- Sodium
- Uric acid
Loss of these substances can lead to a variety of problems. Further tests and a physical exam may show signs of:
- Dehydration due to excess urination
- Growth failure
- Osteomalacia
- Rickets
- Type 2 renal tubular acidosis
Treatment
Many different diseases can cause Fanconi syndrome. The underlying cause and its symptoms should be treated as appropriate.
Outlook (Prognosis)
The prognosis depends on the underlying disease.
When to Contact a Medical Professional
Contact your health care provider if you have dehydration or muscle weakness.
References
Bonnardeaux A, Bichet DG. Inherited disorders of the renal tubule. In: Yu ASL, Chertow GM, Luyckx VA, Marsden PA, Skorecki K, Taal MW, eds. Brenner and Rector's The Kidney. 11th ed. Philadelphia, PA: Elsevier; 2020:chap 44.
Chua AN, Kumar R, Foreman JW. Fanconi syndrome and other proximal tubule disorders. In: Johnson RJ, Floege J, Tonelli M, eds. Comprehensive Clinical Nephrology. 7th ed. Philadelphia, PA: Elsevier; 2024:chap 50.
Review Date: 3/31/2024
Reviewed By: Todd Gersten, MD, Hematology/Oncology, Florida Cancer Specialists & Research Institute, Wellington, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
All rights reserved.