Syndromic cases occur with diseases such as Usher syndrome, Stickler syndrome, Waardenburg syndrome, Alport's syndrome, and neurofibromatosis type 2.
42.
According to a paper published in 2011, the discrepancy in Artaxerxes limb lengths may have arisen as a result of the inherited disease neurofibromatosis.
43.
The claim has recently received support from numismatic and other written evidence suggesting that both Achaemenid and Parthian kings suffered from the hereditary disease neurofibromatosis.
44.
Schwannomas can be associated with neurofibromatosis type II, which may be due to a loss-of-function mutation in the protein merlin.
45.
Shome D, Honavar SG, Vemuganti GK, Reddy VAP . Orbital Embryonal Rhabdomyosarcoma in Association with Neurofibromatosis Type 1-A Case Report.
46.
Other members are Costello syndrome ( CS ), cardio-facio-cutaneous syndrome ( CFC ) and Neurofibromatosis type I ( NF1 ).
47.
The 46-year-old patient, Lucica Bunghez, suffers from neurofibromatosis, a genetic disorder which causes tumors to grow on the body.
48.
Bunghez suffered from neurofibromatosis, or NF, a progressive disorder of the nervous system that causes disfiguring tumors to form on nerves throughout the body.
49.
A condition which shows complete penetrance is neurofibromatosis type 1-every person who has a mutation in the gene will show symptoms of the condition.
50.
Hetezygosity for NF1 ( neurofibromatosis 1 ) tumor suppressor resulting in reduced attachment and spreading and increased motility also coincides with upregulated T-cadherin expression.
