ਆਟੋਇਮਿਊਨ ਰੋਗ ਚਮੜੀ 'ਤੇ ਬਹੁਤ ਸਾਰੇ ਨਿਊਰੋਫਾਈਬਰੋਮਾ ਅਤੇ ਚਟਾਕ ਅਤੇ ਅਕਸਰ ਵਿਕਾਸ ਸੰਬੰਧੀ ਅਸਧਾਰਨਤਾਵਾਂ ਦੁਆਰਾ ਦਰਸਾਏ ਜਾਂਦੇ ਹਨ।,

neurofibromatosis's Usage Examples:

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

Spinal deformities may be caused by birth defects, fractures, marfan syndrome, neurofibromatosis, neuromuscular diseases, severe injuries, and tumors.

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

Sunitinib is being studied for treatment of meningioma which is associated with neurofibromatosis.

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);.

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

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

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

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

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

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

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

Optic nerve glioma (or optic glioma), a form of glioma which affects the optic nerve, is often one of the central nervous system manifestations of neurofibromatosis.