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 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:
- Certain medications, including azathioprine, cidofovir, gentamicin, and tetracycline
- Kidney transplant
- Light chain deposition disease
- Multiple myeloma
- Primary amyloidosis
Symptoms
- Passing large amounts of urine, which can lead to dehydration
- Bone pain
- 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
Call
your health care provider if you have dehydration or muscle weakness.
Alternative Names
De
Toni-Fanconi syndrome
References
Seifter
JL. Potassium disorders. In: Goldman L, Ausiello D, eds. Cecil Medicine.
23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 118.
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