Fitzsimmons-McLachlan-Gilbert syndrome: A very rare syndrome characterized mainly by mental retardation paraplegia and thickened coarse skin on palms and soles. More detailed information about the symptoms, causes, and treatments of Fitzsimmons-McLachlan-Gilbert syndrome is available below.
See full list of 17 symptoms of Fitzsimmons-McLachlan-Gilbert syndrome
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Read more about causes of Fitzsimmons-McLachlan-Gilbert syndrome.
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Fitzsimmons-McLachlan-Gilbert syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Fitzsimmons-McLachlan-Gilbert syndrome, or a subtype of Fitzsimmons-McLachlan-Gilbert syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Fitzsimmons-McLachlan-Gilbert syndrome as a "rare disease".
Source - Orphanet
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