The case of late diagnosis of neurofibromatosis

Rasulova Dilbar Kamoliddinovna Rasulova Munisa Bahtiyarovna Yusupova Iroda Axmadjanovna

dc.contributor.author	Rasulova Dilbar Kamoliddinovna Rasulova Munisa Bahtiyarovna Yusupova Iroda Axmadjanovna
dc.date.accessioned	2023-03-02T06:23:42Z
dc.date.available	2023-03-02T06:23:42Z
dc.date.issued	2023-02
dc.identifier.issn	2347-6915
dc.identifier.uri	http://repository.tma.uz/xmlui/handle/1/6544
dc.description.abstract	Neurofibromatosis is a genetic disorder that causes benign tumors, which developed on nerves, on the spinal cord or in the brain; in rare cases, tumors can become cancerous. Neurofibromatosis is usually diagnosed in childhood or early adulthood, and characterized by neurological manifestations, specific skin changes and orthopedic defects. Complications of neurofibromatosis can include cardiovascular problems, hearing loss, dizziness, loss of vision, weakness of the muscles, severe pain, convulsion. We present a girl 14-year-old patient with late diagnosed neurofibromatosis, who developed central tetraparesis, torticollis and dysphonia.	en_US
dc.language.iso	en	en_US
dc.subject	neurofibromatosis, tumor, mutation, tetraparesis, deformation of bones.	en_US
dc.title	The case of late diagnosis of neurofibromatosis	en_US
dc.type	Article	en_US