| neurofibromatosis |
Inherited disease characterized by benign tumors that may occur anywhere in the body, including the eyelids and orbital portion of the optic nerve. Brown spots and developmental anomalies (especially in the bones, muscles, and abdominal organs) occur. Curvature of the spine can develop.
Ãâó: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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|---|---|
| neurofibromatosis |
set of genetic disorders in which tumors grow on different types of nerves, bone and skin; type 1 is characterized by spots on the skin
Ãâó: www.conquerchiari.org/Glossary.htm
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| neurofibromatosis 1 |
A disorder characterized by developmental changes in the nervous system, skin, bones, and other tissues. Its most distinctive features are the occurrence of multiple benign soft tumors (neurofibromas) and patches of skin pigmentation (caf?au-lait spots).
Ãâó: www.understandingnf1.org/glossary/
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| neurofibromatosis |
Commonly referred to as "NF." A genetic neurological disorder that can cause tumors to form along the nerves. It can lead to deafness and balance problems.
Ãâó: www.nr.edu/cdhh/sotac%20resource%20guide/glossary....
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| neurofibromatosis |
A familial condition characterized by developmental changes in the nervous system, muscles, bones, and skin - the central form (Neurofibromatosis Type 2) may produce bilateral acoustic neuromas
Ãâó: www.anausa.org/glossary.html
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