Examples of 'neurofibromatosis type' in a sentence
Meaning of "neurofibromatosis type"
neurofibromatosis type: This phrase refers to a genetic disorder that causes tumors to grow on nerve tissue. It is categorized into different types based on specific characteristics and symptoms, with neurofibromatosis type I and type II being the most common forms
How to use "neurofibromatosis type" in a sentence
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neurofibromatosis type
There is a strong association between optic glioma and neurofibromatosis type.
Neurofibromatosis type 1 is a very common genetic condition.
Bilateral acoustic neuromas are strongly associated with neurofibromatosis type II.
Neurofibromatosis type 2 is the less common form of neurofibromatosis.
A particular embodiment of the invention embraces the treatment or prevention of neurofibromatosis type I.
I was diagnosed with neurofibromatosis type 1, which my doctor said it was genetic.
Particularly preferred is the treatment or prevention of neurofibromatosis type I.
Treating patients with neurofibromatosis type 2 remains a difficult task.
They are associated with a disease called neurofibromatosis type 1.
Neurofibromatosis type 1 is the main differential diagnosis for macrodystrophia lipomatosa.
Ependymomas are also seen with neurofibromatosis type II.
People with neurofibromatosis type 1 have a high risk of developing NETs.
Meningiomas are also associated with neurofibromatosis type 1.
People of any age with neurofibromatosis type 1 have a higher risk of cancer.
Vestibular schwannomas are linked with neurofibromatosis type 2.
See also
People with neurofibromatosis type 2 are at increased risk to develop tumors within their nerves.
Read more about treating neurofibromatosis type 1.
But neurofibromatosis type 2 only accounts for about 5 percent of acoustic neuroma cases.
Therefore, it is suspected amusia is a frequent finding in neurofibromatosis type 1.
Neuroblastoma is also a feature of neurofibromatosis type 1 and the Beckwith-Wiedemann syndrome.
Cerebrovascular disease is a potentially serious complication in patients with neurofibromatosis type 1.
Read more about the causes of neurofibromatosis type 1 and diagnosing neurofibromatosis type 1.
The disease may be either sporadic or associated with neurofibromatosis type 2.
Breast cancer associated with neurofibromatosis type 1, a case series and review of the literature.
The syndrome is rarely associated with neurofibromatosis type 2.
Children with neurofibromatosis type 2 have cells that do not make merlin as they should.
Vestibular schwannomas are linked to neurofibromatosis type 2.
Children with neurofibromatosis type 1 have cells that do not make neurofibromin as they should.
Pedigree of family with neurofibromatosis type 2.
People with neurofibromatosis type 1 have patches of skin that have a different colour from the rest.
Lovastatin appears to be safe, effective for children with neurofibromatosis type 1.
The neurobiology of learning difficulties, neurofibromatosis type 1 as a model for researching and treating learning disorders.
Examples of syndromes that increase the risk of sarcoma include familial retinoblastoma and neurofibromatosis type 1.
Nearly all people with neurofibromatosis type 2 develop some type of tumor within the nervous system.
Selumetinib granted orphan designation in Europe for neurofibromatosis type 1.
Neurofibromatosis Type 1 can be detected in the methods of the invention.
Mutations of the NF2 gene cause a human autosomal dominant disease called neurofibromatosis type 2.
Neurofibromatosis Type 1 can be detected in the methods described herein.
GISTs can also be seen in familial syndromes such as Carney triad and neurofibromatosis type 1.
Neurofibromatosis type 1 NF1 is one of the most frequent genetic disorders in humans.
Her research career focused on genetic disorders, especially neurofibromatosis type I and facioscapulohumeral muscular dystrophy.
Neurofibromatosis type 1 and Noonan syndrome are also associated with juvenile myelomonocytic leukemia.
Hereditary diseases that provokes the development of tumors throughout the body - Neurofibromatosis type first.
He was diagnosed with neurofibromatosis type I, which causes non-cancerous tumours to grow on nerve tissue.
This makes HI the third most common neurocutaneous disorder, behind neurofibromatosis type 1 and tuberous sclerosis.
Neurofibromatosis type 2, An inherited disease that causes noncancerous growth to appear on the auditory nerve.
In humans, it is a tumor suppressor protein involved in Neurofibromatosis type II.
Elephantiasis, neurofibromatosis type I and Proteus syndrome have all been suggested.
In some embodiments, the neurocutaneous syndrome is neurofibromatosis type I.
Neurofibromatosis type 2 patients are rare, even at reference care centers.
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