Neurofibromatosis with quadruparesis (CROSBI ID 568304)
Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Sabolek, Karla ; Šerić, Vesna ; Čorić, Lejla ; Vargek-Solter, Vesna ; Demarin, Vida
engleski
Neurofibromatosis with quadruparesis
Neurofi bromatosis type-1 also known as von Recklinghausen disease is a hereditary illnes with an autosomal dominant mode of inheritance.Th e condition is characterized by variety of congenital abnormalities of the skin, nervous system, bones or other tissue. Th e diagnosis is usually based on clinical fi ndings. We report a 58- year- old patient presented with progressive quadriparesis and hyperpigmented lesions of the skin also known as café au lait. He suff ered from multiple subcutaneous neural tumors. Spine magnetic resonance imaging showed nodular tumors in cervical and lumbar regions. We discuss the patient`s diagnosis, treatment and prognosis.
Neurofibromatosis type-1; von Recklinghausen disease
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Podaci o prilogu
97-97.
2010.
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objavljeno
Podaci o matičnoj publikaciji
Acta clinica Croatica
0353-9466
Podaci o skupu
International Neuropsychiatric Pula Congress (50 ; 2010)
poster
16.06.2010-19.06.2010
Pula, Hrvatska
Povezanost rada
Kliničke medicinske znanosti