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Doctor insights on: Worst Neurofibromatosis Symptom

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Help! Is it possible to have a lot of cafe au lait spots and not have neurofibromatosis?

Help! Is it possible to have a lot of cafe au lait spots and not have neurofibromatosis?

Possible: NIH diagnostic criteria for NF1 with two or more of following features:1)6 or more café-au-lait macules over 5 mm in diameter prepubertal individuals over 15 mm in greatest diameter in postpubertal. 2) 2or more neurofibromas or one plexiform neurofibroma.3)Freckling in armpit or groin areas4)Optic glioma (optic nerve tumor)5) > 2 Lisch nodules (iris of eye)6)typical bone lesions 7)1deg relative nf1

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Dr. Gerald Mandell
165 Doctors shared insights

Neurofibromatosis (Definition)

A genetic condition characterized by cafe au lait spots, which are pigmented patches of skin, and benign ...Read more


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What are the main symptoms of neurofibromatosis?

What are the main symptoms of neurofibromatosis?

Many manifestations: Commonly nf gradually appears with development of brown flat spots and soft nodules under the skin. The brown (café-au-lai) spots are the main symptom of neurofibromatosis. Freckling of armpits, neurofibromas orsubcutaneous bumps, which increase in number with age. Lisch nodules (hamartomas of iris), gliomas of the optic nerve, skeletal dysplasias with limb abnormalities and scoliosis.

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What symptoms make you think of neurofibromatosis?

What symptoms make you think of neurofibromatosis?

There are 2 froms.: Nf-1 is characterized by tumors on small nerves under the skin. The worst form of this was depicted in a movie called the "elephant man". Tumors on spinal nerves can cause numness and weakness of certain arm or leg muscles. Nf-2 is characterized by brain tumors. The most common form is a tumor on both hearing nerves. Hearing loss, dizzyness, and ringing in the ear are common symptoms of nf-2.

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When does neurofibromatosis symptoms start to develop?

When does neurofibromatosis symptoms start to develop?

It varies: Signs of neurofibromatosis type 1 (nf1) can appear before birth or may not be apparent until well into adulthood. Cafe-au-lait (that's french for coffee with milk) spots are often the first thing to be noticed in children; usually more than 5 spots that are bigger than 1/2 cm. Nf2 is a completely different condition with hearing loss or cataract often the first symptom in the late teens/early 20s.

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I'm scared I might have neurofibromatosis, what symptoms should I be wary of?

Cafe Au Lait spots: Which look like this: http://www. Sciencephoto. Com/media/259913/enlarge. Also, the spot must appear, that is, not be there from birth (that would be a birthmark).

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Sir, lumps are only symptoms of neurofibromatosis?

Many others: There are a number of criteria necessary to make the diagnosis of neurofibromatosis. A relative with the condition, neurofibromas (fleshy bumps), more than 5 brown patches (cafe au lait spots) > 1.5 cm in adults, freckling under the arms and groin, and eye changes (can be diagnosed by an ophthalmologist). There are also many different forms of the condition.

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My son has neurofibromatosis type 1 and he is only 2 years old. What symptoms can I expect?

My son has neurofibromatosis type 1 and he is only 2 years old. What symptoms can I expect?

NF 1 is caused by: Mutations of the NF gene, 17q11.2. Clinical course varies widely depending largely on location & size of brain, skin, eye & other tumors. Initial evaluations by a geneticist, ped. Neurologist, ped. Ophthalmologist, developmental/behavioral pediatrician. & Early Intervention, http://www. Dds. Ca.gov/EarlyStart/home. Cfm., guide management. Learning Disabilities & ADHD are common. See www. Ctf. Org.

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If lumps occur after 19 year and no other symptoms of neurofibromatosis found in early age. Which I seen in wikipidia? But it look like lipoma is it?

If lumps occur after 19 year and no other symptoms of neurofibromatosis found in early age. Which I seen in wikipidia? But it look like lipoma is it?

Need to see it.: You can have one neurofibroma without having neurofibromatosis, but it's more likely, statistically, to be a lipoma. A dermatologist can usually tell the difference just by looking, but a biopsy might be necessary to know for sure. Either way, see a dermatologist so you won't need to worry about it anymore.

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How I physically examine that my lumps are only lipomas not neurofibroma? I have only lumps no other symptoms of neurofibromatosis? My age is 27

How I physically examine that my lumps are only lipomas not neurofibroma? I have only lumps no other symptoms of neurofibromatosis? My age is 27

Other signs with NF1: Some helpful clues in distinguishing the 2: café au lait macules--irregularly shaped, evenly pigmented, brown macules. Most have 6 or more café au lait spots that are 1.5 cm or greater in diameter. Axillary and/or perineal freckling neurofibromas nodules may be brown, pink, or skin colored, soft or firm to the touch, and they may have the pathognomonic buttonhole invagination when pressed on.

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Sir, I have no symptoms of neurofibromatosis and also not in my father and mom but some lumps are in my hand and very few on my thigh, is it lipoma?

Sir, I have no symptoms of neurofibromatosis and also not in my father and mom but some lumps are in my hand and very few on my thigh, is it lipoma?

Possibly: Lipoma is a benign tumor which is the most common cause of lumps under the skin. It has a very typical physical exam and your family doctor should be able to tell you after examining the area whether it is or not.

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What is neurofibromatosis?

What is neurofibromatosis?

Nerve ; brain tumors: Neurofibromatosis, inherited problem, with varying degrees of involvement from mild to severe. Neurofibroma is benign tumor that originates from the nerve cells. Tumors usually arise from nerves in the skin or jut under the skin. Type 1 usually appears in children with brown flat skin spots, freckling in armpits, and soft tumors under the skin and sometimes bone deformity. Type 2 usually brain tumors.

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Could anybody get neurofibromatosis?

Congenital condition: Neurofibromatosis is an autosomal dominant genetic disease, meaning if one of your parents has the disease you have a 50% chance of inheriting the disease. There are also instances of spontaneous mutation in about half of cases where an individual has the disease but it is not seen in family members. Either way, you are born with the condition, but may not see symptoms until later.

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Is neurofibromatosis a rare disease?

Is neurofibromatosis a rare disease?

Define rare: At 1/4000 births this is relatively common compared to many genetically influenced afflictions. About a 3rd are new mutations and the others are passed from an affected parent to half their offspring.

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What are the tests for neurofibromatosis?

Clinical diagnosis: The best test for neutofibromatosis is a physical examination by a practitioner familiar with the nih criteria.

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What is the history of neurofibromatosis?

Long history: Von Recklinghausen's (NF1) has pictorial history, dating back to thirteenth century. In 1768, Akenside published a scientifically-based description of NF1, recognizing that scholars such as Parè and Aldrovandi, in fact suffered from a disorder of the nerves. Neuromas of NF1 were first detailed by Smith in 1849, but Frederick von Recklinghausen is credited with its discovery and coined the name.

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Please help me? What is neurofibromatosis?

Neurofibromatosis: Neurofibromatosis or nf is an inherited disorder or one that occur spontaneously in a patient. It is a disorder that involves the nerves, structures that carry information from the brain to outlying parts of our bodies. In nf there are tumors, which in most cases are benign that arise from these nerves. The disease is extremely variable in how it affects a patient.

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Can neurofibromatosis have a cure someday?

Can neurofibromatosis have a cure someday?

Hopefully Yes: We have learned much about neurofibromatosis (nf) over the years. As our understanding grows our treatments and possibly a cure will come. Our understanding is advancing ever more rapidly in the last few years.

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How can I know if I have neurofibromatosis?

How can I know if I have neurofibromatosis?

Many signs: Physician with physical exam can detect many signs of nf. Symptoms of nf1, most common form may be seen at birth and may include light brown spots on the skin ("cafe-au-lait" spots), two or more growths on the iris of the eye, a tumor of optic nerve, a larger than normal head circumference, development of subcutaneous nodules or neurofibromas, abnormal spine, tibia, or other bone.

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