Abstract | INTRODUCTION: METHODS: Data on neurological presentation and follow-up were gathered from both our patients, homozygous for the G631R mutation in the CP gene, and other published Caucasian cases. Neurological features of aceruloplasminemia in Caucasian patients were compared to those summarized in Japanese patients. RESULTS: CONCLUSIONS:
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Authors | Lena H P Vroegindeweij, Janneke G Langendonk, Mirjam Langeveld, Mels Hoogendoorn, Anneke J A Kievit, Domenico Di Raimondo, J H Paul Wilson, Agnita J W Boon |
Journal | Parkinsonism & related disorders
(Parkinsonism Relat Disord)
Vol. 36
Pg. 33-40
(03 2017)
ISSN: 1873-5126 [Electronic] England |
PMID | 28012953
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2016 Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Adult
- Ceruloplasmin
(deficiency, genetics)
- Female
- Follow-Up Studies
- Humans
- Iron Metabolism Disorders
(diagnostic imaging, epidemiology, genetics)
- Male
- Middle Aged
- Nervous System Diseases
(diagnostic imaging, epidemiology, genetics)
- Neurodegenerative Diseases
(diagnostic imaging, epidemiology, genetics)
- Pedigree
- Phenotype
- White People
(genetics)
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