Literature DB >> 18006953

A novel PANK2 gene mutation: clinical and molecular characteristics of patients short communication.

Beata Kazek1, Ewa Jamroz, Martin Gencik, Aleksandra Jezela Stanek, Elzbieta Marszal, Katarzyna Wojaczynska-Stanek.   

Abstract

Pantothenate kinase-associated neurodegeneration (PKAN) is a progressive neurodegenerative disorder with autosomal recessive inheritance. The major symptoms of PKAN include the onset before the age of 20 years, progressive pyramidal and extrapyramidal signs, retinitis pigmentosa, optic atrophy, dementia, and iron depositions in the globus pallidus. The authors present 3 patients with proven molecular diagnosis of PKAN, in whom 2 novel mutations of PANK2 gene have been identified.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 18006953     DOI: 10.1177/0883073807307092

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  3 in total

Review 1.  Ophthalmic manifestations of inherited neurodegenerative disorders.

Authors:  Hannah M Kersten; Richard H Roxburgh; Helen V Danesh-Meyer
Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

2.  A Novel PANK2 Mutation in a Patient with Atypical Pantothenate-Kinase-Associated Neurodegeneration Presenting with Adult-Onset Parkinsonism.

Authors:  Joo-Hyun Seo; Sook-Keun Song; Phil Hyu Lee
Journal:  J Clin Neurol       Date:  2009-12-31       Impact factor: 3.077

3.  A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome.

Authors:  Myriam Ley Martos; María Jesús Salado Reyes; Rosario Marín Iglesias; Carmen Gutiérrez Moro; Manuel Lubián Gutiérrez; Lorena Estepa Pedregosa
Journal:  J Mov Disord       Date:  2020-07-14
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.