Fanconi Syndrome, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions

Nonfiction, Health & Well Being, Medical, Specialties, Internal Medicine, Nephrology, Health, Ailments & Diseases, Genetic

• Author: Kenneth Kee
• ISBN: 9781370006564
• Publisher: Kenneth Kee
• Publication: July 4, 2017
• Imprint: Smashwords Edition
• Language: English

Fanconi syndrome is a medical disorder of the tubes of the kidney in which some substances normally re-absorbed into the bloodstream by the kidneys are excreted into the urine instead.
Fanconi syndrome indicates the generalized poor function of the kidney’s proximal tubules, not the other nephron segments
Fanconi syndrome results in:

1. Aminoaciduria,
2. Glycosuria,
3. Phosphaturia,
4. Renal tubular acidosis (RTA) type 2 (proximal),
5. Hypophosphatemic rickets (children) or osteomalacia (adults),
6. Renal glycosuria
   It may be inherited or acquired:
   Inherited
7. Primary idiopathic:
   a. Sporadic or familial (autosomal dominant - chromosome 15).
   This occurs in the absence of any identifiable reason, and most cases are sporadic.
   Some cases are genetic, but the mode of inheritance appears to be variable (autosomal-dominant, autosomal-recessive, X-linked).
8. Secondary:
   a. Cystinosis, tyrosinaemia,
   b. Wilson's disease,
   c. Lowe's syndrome (oculo-cerebro-renal syndrome: bilateral congenital cataracts, glaucoma, general hypotonia, hyporeflexia, severe learning disability and Fanconi syndrome),
   d. Galactosemia,
   e. Fructose intolerance,
   f. Glycogen storage disorders and
   g. Mitochondrial cytopathies.
   Acquired
9. Intrinsic renal disease:
   a. Acute tubular necrosis,
   b. Interstitial nephritis,
   c. Hypokalemic nephropathy,
   d. Myeloma,
   e. Amyloidosis,
   f. Sjogren's syndrome,
   g. Rejected transplant.
10. Hyperparathyroidism.
11. Drugs - e.g., cisplatin, ifosfamide, sodium valproate, tenofovir, aminoglycoside antibiotics and deferasirox
12. Toxins:
    a. Glue sniffing,
    b. Heavy metals,
    c. Bee stings
    Causes

Fanconi syndrome can be caused by faulty genes or it may occur later in life due to kidney damage.
Fanconi syndrome is caused by many predominantly rare causes.
The most frequent causes of Fanconi syndrome in children are genetic defects that entail the body's capability to break down some substances such as:

1. Cystine (cystinosis)

2. Fructose (fructose intolerance)

3. Galactose (galactosemia)

4. Glycogen (glycogen storage disease)
   Other causes in children are:

5. Exposure to heavy metals such as lead, mercury, or cadmium

6. Lowe syndrome,

7. Wilson disease
   In adults, Fanconi syndrome can be caused by a range of things that damage the kidneys, such as:

8. Certain medicines, such as azathioprine, cidofovir, gentamicin, and tetracycline

9. Kidney transplant

10. Light chain deposition disease

11. Multiple myeloma

12. Primary amyloidosis
    Symptoms

13. Polyuria, polydipsia, dehydration

14. Bone deformities
    Diagnosis
    The diagnosis is based on too much loss of substances in the urine (e.g., amino acids, glucose, phosphate, bicarbonate) in the absence of high plasma concentrations
    Further tests are needed to identify the cause.

15. Proteinuria: normally, only in small amounts.

16. Hypo-kalemia, hypo-phosphatemia and hyper-chloremic metabolic acidosis
    Further tests and a physical examination may show signs of:

17. Dehydration due to excess urination

18. Growth failure

19. Osteomalacia

20. Rickets

21. Type 2 renal tubular acidosis
    Treatment
    Treatment mainly comprises of the replacement of substances lost in the urine and specific treatment for the underlying cause.
    Treatments of the underlying cause are:

22. Alkali and potassium for RTA (renal tubular acidosis), phosphate and calcitriol for phosphate wasting.

23. Dehydration due to polyuria

24. Metabolic acidosis due to the loss of bicarbonate

25. Thiazide diuretic: may be essential to prevent volume expansion

26. Correction of metabolic acidosis

27. Phosphate and vitamin D supplementation
    Renal losses of glucose, amino acids, and uric acid are not normally symptomatic and do not need replacement.

TABLE OF CONTENT
Introduction
Chapter 1 Fanconi Syndrome
Chapter 2 Causes
Chapter 3 Symptoms
Chapter 4 Diagnosis
Chapter 5 Treatment
Chapter 6 Prognosis
Chapter 7 Glomerulonephritis
Chapter 8 Renal Failure
Epilogue