স্বয়ংক্রিয়ভাবে পিছু প্রভাবশালী রোগ অসংখ্য neurofibromas দ্বারা এবং ত্বকে দাগ দ্বারা এবং প্রায়ই উন্নয়নমূলক অস্বাভাবিকতা দ্বারা চিহ্নিত

neurofibromatosis's Usage Examples:

The three types are neurofibromatosis type I (NF1),.

stand-alone tumors, while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease.

In contrast, Café au lait lesions of neurofibromatosis have smooth borders (“coast of California").

Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.

alter cellular growth control, and neural development, resulting in neurofibromatosis type 1 (NF1, also known as von Recklinghausen syndrome).

In humans, it is a tumor suppressor protein involved in neurofibromatosis type II.

often mistaken for neurofibromatosis type I (NF-1).

It is also known as neurofibromatosis type 1-like syndrome.

sign is the presence of axillary (armpit) freckling in people with neurofibromatosis type I (von Recklinghausen's disease).

cases are diagnosed in people with neurofibromatosis; the lifetime risk for an MPNST in patients with neurofibromatosis type 1 is 8–13%.

The most commonly presented condition is neurofibromatosis Type IIb (45% of cases), followed by neurofibromatosis type IIa (30% of cases).

factors associated with intradural tumors, most commonly neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2), and Von-Hippel Lindau (VHL) syndrome.

studying the genetics of acoustic neuromas in patients with neurofibromatosis, to better understanding how to treat these tumors and prevent their.

the health and well-being of individuals and families affected by neurofibromatosis (NF).

spectrum disorder, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis, LEOPARD syndrome, Crouzon syndrome, Wolf–Hirschhorn syndrome, Andersen–Tawil.

Noonan syndrome is fairly common (1:1,000 to 1:2,500 live births), and neurofibromatosis 1 (which was once thought to be related to NSML) is also common (1:3500);.

neurofibromatosis's Meaning':

autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities