Neurofibromatosis type 1
The most common type of neurofibromatosis. it is characterized clinically by cutaneous and subcutaneous tumors with patches of hyperpigmentation. The hyperpigmented skin areas, are present from birth and found anywhere on the body surface. they can vary markedly in size and color. the dark brown areas are called cafe-au-lait spots. The multiple cutaneous and subcutaneous tumors are nerve sheath tumors, called neurofibromas. they can develop anywhere along the peripheral nerve fibers. Neurofibromas can become quite large, causing a major disfigurement, eroding bone, and compressing various peripheral nerve structures. type 1 neurofibromatosis has dominant inheritance, with a gene locus on the proximal long arm of chromosome 17.
WikiMD Resources - Neurofibromatosis type 1
Science to Social Media | |
|---|---|
WikiMD Resources on Neurofibromatosis type 1 | |
| Uptodate | |
| Medline | |
| Pub Med | |
| Wikipedia | |
| About | |
Social media links on Neurofibromatosis type 1
| |
 Ad. Tired of being overweight?. W8MD's insurance Weight loss program can HELP* |
Quick links: Medicine Portal | Encyclopedia | Gray's Anatomy | Topics | Diseases | Drugs | Wellness | Obesity | Metabolic syndrome | Weight loss*
Disclaimer: The entire contents of WIKIMD.ORG are for informational purposes only and do not render medical advice or professional services. If you have a medical emergency, you should CALL 911 immediately! Given the nature of the wiki, the information provided may not be accurate, misleading and or incorrect. Use the information on this wiki at your own risk! See full Disclaimer.
Link to this page: <a href="http://www.wikimd.org/wiki/Neurofibromatosis_type_1">Neurofibromatosis type 1</a>
- Individual results may vary for weight loss from our sponsors.