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Hartnup Disease ˈhärt-ˌnəp-

(Hartnup's Disease)

By Christopher J. LaRosa, MD, Assistant Professor of Pediatrics;Attending Physician, Division of Pediatric Nephrology, Perelman School of Medicine at The University of Pennsylvania;Children’s Hospital of Philadelphia

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Hartnup disease is a rare hereditary disorder that results in a rash and brain abnormalities because tryptophan and certain other amino acids are not well absorbed from the intestine and not well reabsorbed by the kidneys, so the body has inadequate amounts of these substances.

In Hartnup disease, the transport of amino acids in the intestine and kidneys is disordered. Hartnup disease occurs when a person inherits two copies of the abnormal gene for the disorder, one from each parent. The defective gene controls the absorption of certain amino acids from the intestine and the reabsorption of those amino acids in the kidneys. Consequently, a person with Hartnup disease cannot absorb amino acids properly from the intestine and cannot reabsorb them properly from tubules in the kidneys.

Excessive amounts of amino acids, such as tryptophan, are excreted in the urine. The body is thus left with inadequate amounts of amino acids, which are the building blocks of protein. With too little tryptophan in the blood, the body is unable to make a sufficient amount of the B-complex vitamin niacin, particularly under stress when more vitamins are needed.

Viewing the Urinary Tract

Symptoms

The intestine and kidneys function normally, aside from the problem transporting amino acids, and the effects of the disease occur mainly in the brain and skin. Although the disorder is present at birth, symptoms of Hartnup disease may begin in infancy or childhood, but sometimes they begin as late as early adulthood. Symptoms may be triggered by sunlight, fever, drugs, or emotional or physical stress.

A period of poor nutrition nearly always precedes an attack. Most symptoms occur sporadically and are caused by a deficiency of niacin. The symptoms resemble those caused by a dietary deficiency of niacin (pellagra), particularly the rash that develops on parts of the body exposed to the sun. Intellectual disability, short stature, headaches, an unsteady gait, and collapsing or fainting are common. Psychologic problems (such as anxiety, rapid mood changes, delusions, and hallucinations) may also result.

Diagnosis

  • Urine tests

Laboratory tests done on urine samples reveal an abnormally high excretion of amino acids and their by-products (such as serotonin).

Prognosis

The prognosis for Hartnup disease is good, and the attacks usually become progressively less frequent with age.

Treatment

  • Protein and niacin in the diet

  • Supplements of nicotinamide (niacinamide) or niacin (nicotinic acid)

  • For attacks, nicotinamide

  • Avoiding sun exposure and sulfonamides

People with Hartnup disease can reduce the number and severity of attacks by maintaining good nutrition and eating enough protein and supplementing their diet with niacinamide or niacin (a B-complex vitamin very similar to niacinamide). People may take nicotinamide to treat attacks.

People who have Hartnup disease also should avoid sun exposure as well as antibiotics that contain sulfonamides.

Resources In This Article

Drugs Mentioned In This Article

  • Generic Name
    Select Brand Names
  • NIACOR, NIASPAN
  • No US brand name

* This is the Consumer Version. *