How Do You Spell NEUROFIBROMATOSIS?

Pronunciation: [njˌuːɹəfˌɪbɹəmɐtˈə͡ʊsɪs] (IPA)

Neurofibromatosis is a genetic disorder that affects the development of nerve cells and causes the growth of tumors on the nerves. The word is spelled as "ˌnjʊəroʊfaɪbrəʊməˈtoʊsəs" using IPA phonetic transcription to help with its pronunciation. The "neuro-" prefix refers to nerves, while "fibroma" means tumors made of fibrous tissue. The suffix "-tosis" refers to a condition of abnormal growth. Overall, neurofibromatosis is a complex word that accurately describes the condition it represents.

NEUROFIBROMATOSIS Meaning and Definition

1. Neurofibromatosis is a genetic disorder characterized by the development of noncancerous tumors, known as neurofibromas, throughout the nervous system. It is caused by mutations or alterations in specific genes that control cell growth and division. There are three types of neurofibromatosis: neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis.

   In NF1, which is the most common type, symptoms typically manifest in childhood and may include café-au-lait spots on the skin, soft and benign tumors on or under the skin, and skeletal abnormalities such as scoliosis. NF2, on the other hand, is characterized by the development of tumors on the nerves responsible for hearing and balance. Schwannomatosis is the rarest form of neurofibromatosis and leads to the growth of multiple schwannomas, which are usually benign tumors arising from the Schwann cells that form the protective covering of nerves.

   Neurofibromatosis is a lifelong condition with varying degrees of severity, as symptoms can range from mild to severe, even within the same family. The disorder is typically diagnosed through a thorough clinical examination and confirmed through genetic testing. While there is currently no cure for neurofibromatosis, treatment aims to manage symptoms and complications. Depending on the specific case, treatment options may include surgical removal of tumors, physical therapy, medication, and regular monitoring to detect any potential complications or tumor growth.

   Overall, neurofibromatosis is a complex genetic disorder characterized by the development of noncancerous tumors throughout the nervous system, with varying symptoms and severity depending on the type and individual case.

2. 1. The occurrence of tumors due to circumscribed hyperplasia of the fibrous structure of the nerves. 2. Recklinghausen's disease, of which it is one of the manifestations.

   A practical medical dictionary. By Stedman, Thomas Lathrop. Published 1920.

Common Misspellings for NEUROFIBROMATOSIS

• beurofibromatosis
• meurofibromatosis
• jeurofibromatosis
• heurofibromatosis
• nwurofibromatosis
• nsurofibromatosis
• ndurofibromatosis
• nrurofibromatosis
• n4urofibromatosis
• n3urofibromatosis
• neyrofibromatosis
• nehrofibromatosis
• nejrofibromatosis
• neirofibromatosis
• ne8rofibromatosis
• ne7rofibromatosis
• neueofibromatosis
• neudofibromatosis
• neufofibromatosis
• neuriofibromatosis

Etymology of NEUROFIBROMATOSIS

The word "neurofibromatosis" is derived from the combination of three components: "neuro", "fibro", and "matosis".

1. "Neuro" originates from the Greek word "neuron", meaning "nerve".

2. "Fibro" comes from the Latin word "fibra", which means "fiber" or "thread".

3. "Matosis" is derived from the Greek word "matos", referring to "a growth" or "proliferation".

When these components are combined, "neurofibromatosis" refers to a condition characterized by multiple tumors or growths (fibromas) that affect the nerves (neuro) throughout the body.

Plural form of NEUROFIBROMATOSIS is NEUROFIBROMATOSES