Cargando…
Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series
INTRODUCTION: Paroxysmal kinesigenic dyskinesia is characterized by sudden attacks of involuntary movements. It is often misdiagnosed clinically as psychogenic illness, which distresses the patients to a great extent. A correct diagnosis will improve the quality of life in patients with paroxysmal k...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077686/ https://www.ncbi.nlm.nih.gov/pubmed/24886244 http://dx.doi.org/10.1186/1752-1947-8-174 |
_version_ | 1782323634388336640 |
---|---|
author | Matsumoto, Naoya Takahashi, Satoru Okayama, Akie Araki, Akiko Azuma, Hiroshi |
author_facet | Matsumoto, Naoya Takahashi, Satoru Okayama, Akie Araki, Akiko Azuma, Hiroshi |
author_sort | Matsumoto, Naoya |
collection | PubMed |
description | INTRODUCTION: Paroxysmal kinesigenic dyskinesia is characterized by sudden attacks of involuntary movements. It is often misdiagnosed clinically as psychogenic illness, which distresses the patients to a great extent. A correct diagnosis will improve the quality of life in patients with paroxysmal kinesigenic dyskinesia because treatment with low doses of anticonvulsants is effective for eliminating the clinical manifestations. Paroxysmal kinesigenic dyskinesia can occur independently of or concurrently with benign infantile convulsion. Identification of PRRT2 as the causative gene of benign infantile convulsion and paroxysmal kinesigenic dyskinesia allows genetic confirmation of the clinical diagnosis. CASE PRESENTATION: We describe the clinical features of a Japanese family with either paroxysmal kinesigenic dyskinesia or benign infantile convulsion. A PRRT2 missense mutation (c.981C > G, p.Ile327Met) was identified in two patients with benign infantile convulsion and three patients with paroxysmal kinesigenic dyskinesia as well as in two unaffected individuals. Allowing incomplete penetrance in the mutation carriers, this mutation co-segregated completely with the phenotype. The patients with paroxysmal kinesigenic dyskinesia had been misdiagnosed with psychogenic illness for many years. They were correctly diagnosed with paroxysmal kinesigenic dyskinesia when their children visited a pediatrician for benign infantile convulsion. Treatment with carbamazepine controlled their involuntary movements completely. CONCLUSIONS: Paroxysmal kinesigenic dyskinesia is a treatable movement disorder that is often misdiagnosed clinically as psychogenic illness. It is important to note that two clinically distinct disorders, benign infantile convulsion and paroxysmal kinesigenic dyskinesia, are allelic conditions caused by PRRT2 mutations. Paroxysmal kinesigenic dyskinesia should be suspected in families with a child with benign infantile convulsion. |
format | Online Article Text |
id | pubmed-4077686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40776862014-07-02 Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series Matsumoto, Naoya Takahashi, Satoru Okayama, Akie Araki, Akiko Azuma, Hiroshi J Med Case Rep Case Report INTRODUCTION: Paroxysmal kinesigenic dyskinesia is characterized by sudden attacks of involuntary movements. It is often misdiagnosed clinically as psychogenic illness, which distresses the patients to a great extent. A correct diagnosis will improve the quality of life in patients with paroxysmal kinesigenic dyskinesia because treatment with low doses of anticonvulsants is effective for eliminating the clinical manifestations. Paroxysmal kinesigenic dyskinesia can occur independently of or concurrently with benign infantile convulsion. Identification of PRRT2 as the causative gene of benign infantile convulsion and paroxysmal kinesigenic dyskinesia allows genetic confirmation of the clinical diagnosis. CASE PRESENTATION: We describe the clinical features of a Japanese family with either paroxysmal kinesigenic dyskinesia or benign infantile convulsion. A PRRT2 missense mutation (c.981C > G, p.Ile327Met) was identified in two patients with benign infantile convulsion and three patients with paroxysmal kinesigenic dyskinesia as well as in two unaffected individuals. Allowing incomplete penetrance in the mutation carriers, this mutation co-segregated completely with the phenotype. The patients with paroxysmal kinesigenic dyskinesia had been misdiagnosed with psychogenic illness for many years. They were correctly diagnosed with paroxysmal kinesigenic dyskinesia when their children visited a pediatrician for benign infantile convulsion. Treatment with carbamazepine controlled their involuntary movements completely. CONCLUSIONS: Paroxysmal kinesigenic dyskinesia is a treatable movement disorder that is often misdiagnosed clinically as psychogenic illness. It is important to note that two clinically distinct disorders, benign infantile convulsion and paroxysmal kinesigenic dyskinesia, are allelic conditions caused by PRRT2 mutations. Paroxysmal kinesigenic dyskinesia should be suspected in families with a child with benign infantile convulsion. BioMed Central 2014-06-01 /pmc/articles/PMC4077686/ /pubmed/24886244 http://dx.doi.org/10.1186/1752-1947-8-174 Text en Copyright © 2014 Matsumoto et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Matsumoto, Naoya Takahashi, Satoru Okayama, Akie Araki, Akiko Azuma, Hiroshi Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title | Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title_full | Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title_fullStr | Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title_full_unstemmed | Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title_short | Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
title_sort | benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077686/ https://www.ncbi.nlm.nih.gov/pubmed/24886244 http://dx.doi.org/10.1186/1752-1947-8-174 |
work_keys_str_mv | AT matsumotonaoya benigninfantileconvulsionasadiagnosticclueofparoxysmalkinesigenicdyskinesiaacaseseries AT takahashisatoru benigninfantileconvulsionasadiagnosticclueofparoxysmalkinesigenicdyskinesiaacaseseries AT okayamaakie benigninfantileconvulsionasadiagnosticclueofparoxysmalkinesigenicdyskinesiaacaseseries AT arakiakiko benigninfantileconvulsionasadiagnosticclueofparoxysmalkinesigenicdyskinesiaacaseseries AT azumahiroshi benigninfantileconvulsionasadiagnosticclueofparoxysmalkinesigenicdyskinesiaacaseseries |