Myhre Syndrome: A very rare inherited disorder characterized by retarded growth, mental retardation, bone abnormalities and distinctive facial features. More detailed information about the symptoms, causes, and treatments of Myhre Syndrome is available below.
See full list of 20 symptoms of Myhre Syndrome
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Medical news articles related to Myhre Syndrome include:
Source: HealthDay News
Read more about complications of Myhre Syndrome.
Read more about causes of Myhre Syndrome.
Research the causes of these diseases that are similar to, or related to, Myhre Syndrome:
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
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Mental retardation, growth deficiency, midfacial hypoplasia, hearing loss, generalized muscular hypertrophy, joint limitation, and skeletal abnormalities are the cardinal features of this syndrome. See also Myhre-GOMBO syndrome. - (Source - Diseases Database)
Myhre Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Myhre Syndrome, or a subtype of Myhre Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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