Living with idiopathic basal ganglia calcification 3: a qualitative study describing the lives and illness of people diagnosed with a rare neurological disease

PURPOSE: Idiopathic basal ganglia calcification (IBGC) is a rare, intractable disease with unknown etiology. IBGC3 is a familial genetic disease defined by genetic mutations in the major causative gene (SLC20A2). People with IBGC3 experience distress from the uncommon nature of their illness and unc...

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Detalles Bibliográficos
Autores principales: Takeuchi, Tomiko, Muraoka, Koko, Yamada, Megumi, Nishio, Yuri, Hozumi, Isao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050183/
https://www.ncbi.nlm.nih.gov/pubmed/27777849
http://dx.doi.org/10.1186/s40064-016-3390-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050183/
https://www.ncbi.nlm.nih.gov/pubmed/27777849
http://dx.doi.org/10.1186/s40064-016-3390-z

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