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Alstrom Syndrome


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This WisdomCard managed by: Tara Salamone

Alstrom syndrome is a rare genetic disorder. It affects multiple organs of the body.1 It is a progressive disease, with extreme light sensitivity (photophobia), and a wobbling of the eyes (nystagmus), occuring in infancy. Later in life, complications such as blindness, type 2 diabetes, heart failure, hearing impairment, liver disease develop.2

Fast Facts:

  • --Presently, approximately 425 people worldwide are known to be have this disease.1
  • --Named after C.H. Alström, who described the condition in Sweden in 1959.3
  • -- The gene is recessive, which means it must be passed from both parents for the syndrome to manifest.1

5 Great Resources on Alstrom Syndrome

5 Latest Headlines on Alstrom Syndrome

What is Alstrom Syndrome?

What Are The Symptoms of Alstrom Syndrome?

What Are The Causes and Complications of Alstrom Syndrome?

What Are The Treatments and Medications for Alstrom Syndrome?

What Are The Types, Stages and Survival Rates of Alstrom Syndrome?

Wisdom, Blogs, and Message Boards about Alstrom Syndrome

Foundations and Support Groups on Alstrom Syndrome

Scientific and Medical Journal Articles on Alstrom Syndrome

Clinical Trials on Alstrom Syndrome

Related WisdomCards

GuideWisdom and Fast Facts References

  1. 1.0 1.1 1.2 Genetics Home Reference: What is Alstrom Syndrome
  2. MedTerms (via MedicineNet): Definition of Alstrom Syndrome
  3. Wikipedia: Alstrom Syndrome

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