Neurofibromatosis I (NF-I): features on MRI

Neurofibromatosis (or von Recklinghausen disease) is a hereditary condition due to mesodermal and neuroectodermal dysplasia, eponymously named after the researcher who reported it in 1882. The disorder is transmitted as an autosomal dominant condition, but 50% of cases arise as spontaneous mutations. The incidence falls within the range 1:2 000 - 1:4 000, and has no gender bias. We present a series of images produced by different modalities that show lesions and pathologies that are characteristic of the disease.

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Neurofibromatosis revisited: A pictorial review

Khan

Werke

Ismail

2010

S. Afr. j. radiol.

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Neurofibromatosis I (NF-I): features on MRI

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Neurofibromatosis revisited: A pictorial review

Neurofibromatosis revisited: A pictorial review

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