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    Neurology. 2005 May 24;64(10):1810-2.

    The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration.

    Pellecchia MT, Valente EM, 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.

    Source

    Department of Neurological Sciences, University Federico II, Naples, Italy. pellec3@hotmail.com

    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.

    PMID:
    15911822
    [PubMed - indexed for MEDLINE]

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