neurofibromatosis वाक्य
उदाहरण वाक्य
मोबाइल
- However, they may be associated with syndromes such as Neurofibromatosis Type 1 and McCune-Albright syndrome.
- The Folks'cousin, Blake Robinson, was diagnosed with neurofibromatosis when at eighteen months of age.
- The National Neurofibromatosis Foundation honored him in 1986 for his " invaluable contributions " to the field.
- Diamante explico que, en los casos de neurofibromatosis, la mayor capacidad de audicion depende de varios factores.
- Since infancy, Elchonon Hellinger has suffered from Neurofibromatosis Type 2, which causes the continuous growth of benign tumors.
- El implante es el primero en America Latina, en donde infermedades del oido del tipo neurofibromatosis afectan miles de personas.
- "' Neurofibromatosis type II "'is a genetic condition which may be inherited or may arise spontaneously.
- Schwannomas are mostly benign tumors that commonly occur in individuals with NF2 and schwannomatosis ( sometimes called neurofibromatosis type III ).
- As neurofibromatosis poses a greater threat to infants than to adults, the doctor strongly advised them not to have children.
- The " Brainy Camps " are camps for children and teens with Tourette Syndrome, Aspergers, Neurofibromatosis, or Epilepsy.
- Despite harboring molecular abnormalities of the long arm of chromosome 22, intraneural perineurioma has not been associated with neurofibromatosis ."
- He says that the region linked with MS is different from the one, also on chromosome 17, linked to neurofibromatosis.
- Her brother Aaron who was diagnosed with neurofibromatosis died in 2011 of a brain tumor, at the age of 30.
- Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop.
- The neurofibromatosis gene was patented by the University of Michigan, with the initial filing in 1991 and the patent granted in 2001.
- Her clinical research is focused on cognitive deficits in neurofibromatosis type 1 and intervention strategies for children with learning disabilities and inherited myopathies.
- Este tipo de implante permite recuperar la audicion a quienes sufren de una enfermedad infrecuente de caracter hereditario, llamada neurofibromatosis central tipo 2.
- Caf?au lait spots are often harmless, but may be associated with syndromes such as Neurofibromatosis Type 1 and McCune-Albright syndrome.
- In addition to neurofibromatosis type I, mutations in NF1 can also lead to juvenile myelomonocytic leukemia, Watson syndrome, and breast cancer.
- One family, reportedly, so ostracized a child who had the gene for neurofibromatosis that he had to be placed in a foster home.
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