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#legius_syndrome

Legius syndrome

Medical condition

Legius syndrome (LS) is an autosomal dominant condition characterized by cafe au lait spots. It was first described in 2007 and is often mistaken for neurofibromatosis type I. It is caused by mutations in the SPRED1 gene. It is also known as neurofibromatosis type 1-like syndrome.

Sat 24th

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Legius syndrome List of syndromes Neurofibromatosis Macrocephaly Neurofibromatosis type I Polydactyly Micrognathism Phakomatosis Café au lait spot Crowe sign
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