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Search: authors:"László Szpisjak"

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Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene—case series

ObjectiveThe prevalence of xeroderma pigmentosum (XP) is quite low in Europe, which may result in a delay in determining the appropriate diagnosis. Furthermore, some subtypes of XP, including XPA, may manifest themselves with quite severe neurological symptoms in addition to the characteristic dermatological lesions. Accordingly, the aim of the current study is to highlight the...