nf1 disease - Axtarish в Google
10 сент. 2024 г. · Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue.
Neurofibromatosis type 1 (NF1) is a genetic condition that causes tumours to grow along your nerves. The tumours are usually non-cancerous (benign) but may ...
NF-1 causes tumors along the nervous system which can grow anywhere on the body. NF-1 is one of the most common genetic disorders and is not limited to any ...
Нейрофиброматоз I типа Заболевание
Нейрофиброматоз I типа — самое распространённое наследственное заболевание, предрасполагающее к возникновению опухолей у человека. Описан во второй половине XIX века рядом исследователей, в том числе в 1882 году учеником Рудольфа Вирхова Фридрихом... Википедия
МКБ-10 : Q85.0
МКБ-11 : LD2D.10
МКБ-9 : 237.71
OMIM : 162200
1 июл. 2020 г. · Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along nerves in the skin, brain, and ...
Neurofibromatosis type 1 is one of the most common inherited disorders and can primarily the skin, nervous system and eyes.
Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple café au lait macules, intertriginous freckling, multiple cutaneous neurofibromas,
25 апр. 2022 г. · Neurofibromatosis 1 (NF1), historically called von Recklinghausen's disease, is a genetic disorder characterized by increased risk of developing ...
NF1 affects how often certain cells grow in your body. This leads to the formation of benign (noncancerous) tumors. These specifically are nerve tumors called ...
10 сент. 2024 г. · This genetic condition causes tumors on nerve tissue. Surgery and other therapies can manage symptoms.
NF1 is a variable disorder, which means that it can affect children in many different ways. It usually causes freckles or spots, most often on the skin or eyes.
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