How To Use Neurofibromatosis In A Sentence
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Google responded with items suggesting the man had neurofibromatosis type 1, the correct diagnosis.
Times, Sunday Times
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Neurofibromatosis is an unusual condition which is often handed down through families.
The Sun
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Lumenis 'state of the art laser system, was used by Dr. Paul Castellanos to perform Trans-oral Laser Microsurgery (TLM) for the treatment of airway stenosis with obstructing neurofibromatosis of the laryngopharynx on a
THE MEDICAL NEWS
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Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before.
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The intracranial tumors associated with neurofibromatosis include optic gliomas, other astrocytomas, neurilemomas, acoustic neuromas, neurofibromas, and meningiomas.
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Dr. Fisher is also using PET and MRI techniques to predict the clinical behavior of plexiform neurofibromas, the largest and most important tumors seen in neurofibromatosis.
Pediatric cancer research
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This freckling is not seen in patients without neurofibromatosis.
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The intracranial tumors associated with neurofibromatosis include optic gliomas, other astrocytomas, neurilemomas, acoustic neuromas, neurofibromas, and meningiomas.
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The other has neurofibromatosis, a genetic condition affecting the nervous system.
The Sun
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Examples of autosomal dominant single gene disorders include: Marfan syndrome, achondroplasia, neurofibromatosis, and retinitis pigmentosa.
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Also at risk of glaucoma are children with neurofibromatosis and Sturge-Weber syndrome.
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In humans, epilepsy is often one of a set of symptoms found in people with diseases such as cerebral palsy, neurofibromatosis, autism, tuberous sclerosis, and Landau-Kleffner syndrome.
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Examples of autosomal dominant single gene disorders include: Marfan syndrome, achondroplasia, neurofibromatosis, and retinitis pigmentosa.
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Neurofibromatosis is one of autosomal - dominant neurogenetic diseases with relatively low incidence.
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Because these mice have one defective copy of the NF1 gene, similar to children with neurofibromatosis 1, the cells make fewer copies of the gene's protein, neurofibromin.
WUSTL Record: University News
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The neurocutaneous syndromes, including neurofibromatosis, tuberous sclerosis and von Hippel-Landau disease, are associated with an increased risk of brain tumors.
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At the age of four, he developed a swelling on his face and had an extreme form of neurofibromatosis diagnosed.
Times, Sunday Times
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The skin must be examined for signs of neurocutaneous syndrome, particularly neurofibromatosis and tuberous sclerosis, which are highly associated with intracranial neoplasms.
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Neurofibromatosis type 1 is a common autosomal dominant disorder with a high rate of penetrance. It is caused by the mutation of the tumor suppressor gene NF1, which encodes neurofibromin.
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Both sisters were born with neurofibromatosis, but were told the tumours are not related.
The Sun
