Rasmussen-Johnsen-Thomsen syndrome: A very rare syndrome characterized mainly by the lack of an ear canal opening as well as foot deformities. More detailed information about the symptoms, causes, and treatments of Rasmussen-Johnsen-Thomsen syndrome is available below.
See full list of 9 symptoms of Rasmussen-Johnsen-Thomsen syndrome
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Types of Rasmussen-Johnsen-Thomsen syndrome
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Rasmussen-Johnsen-Thomsen syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Rasmussen-Johnsen-Thomsen syndrome, or a subtype of Rasmussen-Johnsen-Thomsen 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 Rasmussen-Johnsen-Thomsen syndrome as a "rare disease".
Source - Orphanet
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