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Primrose syndrome is a rare, slowly progre … Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's by Dr D.A.A. Primrose. Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.unknown and there are no known treatments.
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Primrose syndrome is inherited via an autosomal dominant manner
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Intellectual disability-cataracts-calcified pinnae-myopathy syndrome
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| rdfs:comment |
Primrose syndrome is a rare, slowly progre … Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's by Dr D.A.A. Primrose. Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.unknown and there are no known treatments.
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Primrose syndrome
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