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Medical Disclaimer
The medical information on this site is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information is not intended to be patient education, does not create any patient-physician relationship, and should not be used as a substitute for professional diagnosis and treatment.
Neurofibromatosis type 1
Neurofibromatosis 1 (NF1)Von Recklinghausen Disease
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Overview
Neurofibromatosis type 1 (NF1) is an inherited condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along nerves in the skin, brain, and other parts of the body. The signs and symptoms of this condition vary widely among affected people. Mutations in the NF1 gene cause neurofibromatosis type 1. This condition is considered to have an autosomal dominant pattern of inheritance. Source: Genetic and Rare Diseases Information Center (GARD), supported by ORDR-NCATS and NHGRI.
Trusted Medical Sites
Genetic & Rare Diseases Information Center (GARD)
GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.
Support Organizations
Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.
Disease Resources
Resources can help guide your quest for factual and reliable information.
General NF and NF Midwest blog
Blog with frequent postings.
Understanding NF Booklet
Simple booklet explaining what NF1, NF2, and schwannomatosis are.
Finding an NF Specialist or Doctor
Includes information on how to find a doctor for NF or Schwannomatosis
NF1 Resources and Articles
NF1 resources and articles are added frequently. Includes "Be iNFormed" articles that have been written by experts for the lay audience on various complications and concerns of NF1.
Understanding Neurofibromatosis
Booklet for individuals who have been recently diagnosed with NF.