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izvor podataka: crosbi

Neurofibromatosis with quadruparesis (CROSBI ID 568304)

Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija

Sabolek, Karla ; Šerić, Vesna ; Čorić, Lejla ; Vargek-Solter, Vesna ; Demarin, Vida Neurofibromatosis with quadruparesis // Acta clinica Croatica. 2010. str. 97-97

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

Poveznice
Indeksiranost