Fanconi Bickel Syndrome

Fanconi Bickel syndrome is a rare genetic condition affecting galactose metabolism.

About Fanconi Bickel Syndrome (FBS)

Why it is Problematic

Causes and Risk Factors

Symptoms

Diagnosis

Treatment and Prevention

Incidence

 

About Fanconi Bickel Syndrome (FBS)

Fanconi Bickel syndrome is a rare glycogen storage disease characterized by glycogen accumulation in the liver and kidneys caused by impaired carbohydrate metabolism, resulting in impaired galactose metabolism and severe renal tube dysfunction. Fanconi Bickel syndrome is an autosomal recessive disorder requiring one copy from each parent or 2 mutated copies total (homozygous) to express the traits of the disease. Individuals with compound heterozygous mutations, or one copy of more than one mutation on the responsible gene, can also express the traits of Fanconi Bickel syndrome. Carriers, individuals with only one copy (heterozygous) for the mutation, do not have Fanconi-Bickel syndrome.

 

Why it is Problematic

The onset of Fanconi Bickel syndrome often appears in the first year of life. FBS is marked by the inability to thrive. By the age of 2, an affected individual often has an enlarged liver and kidneys and possibly rickets, a condition that makes bones pliable, weak, and prone to bending. FBS can also cause dwarfism.

 

Causes and Risk Factors

Fanconi Bickel syndrome is an inherited genetic disorder. Mutations in the GLUT2 gene have been linked to FBS. Additionally, FBS has been linked to children with parents who are blood related (consanguineous).

 

Symptoms

Initial symptoms usually appear between the age of 3 and 10 months and they include:

  • Failure to grow
  • Failure to thrive
  • Fever
  • Vomiting
  • Glucose (sugar) in urine
  • Normal or slightly enlarged liver at birth
  • Polyuria (excessive urination)
  • Galactose intolerance (type of sugar found in dairy products, a part of lactose)

Other symptoms that appear after the initial symptoms include:

  • Protruding abdomen
  • Enlarged liver
  • Abnormal fat deposits around shoulders and abdomen
  • Dwarfism
  • Moon-shaped face
  • Delayed puberty

Complications associated with the symptoms of  Fanconi-Bickel syndrome include bone fractures, pancreatitis (pancreas swelling), and osteoporosis (weakening of the bones).

 

Diagnosis

Fanconi Bickel syndrome can be detected during neonatal testing. Because patients with FBS are intolerant to galactose, a type of sugar found in lactose-containing dairy products, among other sources, a neonatal test checking for galactose intolerance can help diagnosis FBS.

An X-ray is used to examine bones for patterns of rickets.

Urine tests can measure glycose, phosphates, amino acids, and bicarbonate levels in the body.

A liver biopsy can detect abnormal galactose oxidation.

 

Treatment and Prevention

There is no fully effective treatment for Fanconi Bickel syndrome. Supplement treatments consisting of water, electrolytes, and vitamin D may be used in combination with a galactose-restricted diet. A diet that is low in sugar and carbohydrates and small, frequent meals is recommended. Following these guidelines can improve growth rates and enhance the quality of life for the patient.

 

Incidence

There is little information about Fanconi Bickel syndrome because it is so rare. The exact incidence of FBS has not been determined, but it is believed to occur in less than 1 in one million births.

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