Data di Pubblicazione:
2005
Abstract:
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare autosomal-recessive disorder caused by mutations in the PANK2 gene. The authors report clinical and genetic findings of 16 patients with PKAN. The authors identified 12 mutations in the PANK2 gene, five of which were new. Only nine patients could be classified as classic or atypical PKAN, and intermediate phenotypes are described. Two patients presented with motor tics and obsessive-compulsive behavior suggestive of Tourette syndrome.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Pellecchia, Mt; Valente, ENZA MARIA; Cif, L; Salvi, S; Albanese, A; Scarano, V; Bonuccelli, U; Bentivoglio, Ar; D'Amico, A; Marelli, C; Di Giorgio, A; Coubes, P; Barone, P; Dallapiccola, B.
Link alla scheda completa:
Pubblicato in: