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Article

Neurofibromatosis 1 in childhood.

Seminars in pediatric neurology - 1 Dec 1998

North K N

Abstract excerpt

Neurofibromatosis 1 (NF1) is an autosomal-dominant disorder with an incidence of approximately 1 in 3,000. The cardinal features of the disorder are cafe au lait spots, axillary freckling, cutaneous neurofibromas, and iris hamartomas (Lisch nodules). Common complications include learning disability, scoliosis, and optic gliomas. Other complications (e.g., peripheral nerve malignancy, bony deformities, and...

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Identifiers

PMID: 9874851
DOI: 10.1016/s1071-9091(98)80002-8

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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