copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
Input Form:Deal with this potential dealer,buyer,seller,supplier,manufacturer,exporter,importer
(Any information to deal,buy, sell, quote for products or service)
Neurofibromatosis type 1 - Symptoms and causes - Mayo Clinic Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue Skin changes include flat, light brown spots and freckles in the armpits and groin
Neurofibromatosis type 1 - Diagnosis and treatment - Mayo Clinic To diagnose neurofibromatosis type 1 (NF1), a healthcare professional begins with a review of your personal and family medical history and a physical exam Your child's skin is checked for cafe au lait spots, which can help diagnose NF1
Neurofibromatosis tipo 1 - Síntomas y causas - Mayo Clinic La neurofibromatosis tipo 1 (NF1) es una afección genética que causa cambios en la pigmentación de la piel y tumores en el tejido nervioso Los cambios en la piel incluyen manchas sin relieve de color marrón claro y pecas en las axilas y en la ingle
Neurofibroma - Symptoms and causes - Mayo Clinic A neurofibroma can arise with no known cause, or it may appear in people with a genetic condition called neurofibromatosis type 1 Neurofibromas most often are found in people ages 20 to 30 years old
Neurofibromatosis Type 2 Clinic - Overview - Mayo Clinic Neurofibromatosis type 2 (NF2) is an uncommon genetic condition that results in the development of multiple brain tumors and spinal tumors Almost all people with NF2 have two tumors affecting each of the hearing nerves, called vestibular schwannomas
Neurofibroma - Diagnosis and treatment - Mayo Clinic Selumetinib (Koselugo) has been approved to treat a plexiform neurofibroma in children with neurofibromatosis type 1 A plexiform neurofibroma grows on many nerves The medicine can shrink the tumor Surgery to remove the tumor Symptoms can be relieved by removing all or part of a neurofibroma that's pressing on nearby tissue or damaging organs
Neurofibromatosis type 1 care at Mayo Clinic Mayo Clinic's world-renowned Neurofibromatosis Clinic provides coordinated care for people with this complex condition Geneticists, adult and pediatric neurologists, neuro-oncologists, radiologists, and neurosurgeons work together to provide exactly the care you need
Neurofibromatosis and Schwannomatosis Clinic Overview We provide clinical evaluations for neurofibromatosis type 1 and schwannomatosis (including NF2 related schwannomatosis), and all of our physicians have significant experience treating patients with these rare and complex conditions
Neurofibromatosis type 1 - Doctors and departments - Mayo Clinic Mayo Clinic researchers study genetics, causes and new treatments for people with neurofibromatosis type 1 Research is conducted by Mayo Clinic researchers in clinical genomics, pediatric genetics and neurology