Definition
Alström syndrome is an inherited disease marked by blindness, deafness, diabetes, and obesity.
Causes, incidence, and risk factors
Alström syndrome is an autosomal recessive inherited disorder, which means that a person must inherit a copy of the defective gene from both parents in order to be affected. It is extremely rare, but is more common in Holland and Sweden than in the United States.
The mutated gene, ALMS1, has been identified, but it is not yet known how this gene causes the disorder.
Signs and tests
An ophthalmologist will examine the eyes. The patient may have reduced vision.
Tests may be done to check:
- Triglyceride levels
- Blood sugar levels (to diagnose hyperglycemia)
- Thyroid function
- Hearing
- Heart function (echocardiogram may be abnormal)
Treatment
There is no specific treatment for this syndrome. Treatment for specific symptoms may include:
- Diabetes medication
- Hearing aids
- Heart medications
- Thyroid hormone replacement
Support Groups
Alström Syndrome International --
Expectations (prognosis)
Permanent blindness, deafness, and type 2 diabetes are likely to develop. Kidney and liver failure may get worse.
Complications
Complications related to diabetes can occur. Impaired heart function, if untreated, can lead to fatigue and shortness of breath. Diabetes and high cholesterol increase the risk of coronary artery disease.
Calling your health care provider
Call your health care provider if you suspect symptoms of diabetes such as increased thirst and urination. Seek medical attention promptly if you suspect that your infant or child cannot see or hear normally.
| • | Blindness |
| • | Hearing loss |
| • | Diabetes |
| • | Obesity |
| • | Autosomal recessive |
Reviewed By: Ian Marshall, MD, Division of Pediatric Endocrinology, UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ. Review provided by VeriMed Healthcare Network.
