Primary Familial Brain Calcification Caused by a Novel Compound Heterozygous Mutation in the MYORG Gene.
Acta Neurol Taiwan
; 31(2): 77-79, 2022 Mar 25.
Article
em En
| MEDLINE
| ID: mdl-35266134
BACKGROUND PURPOSE: To demonstrate a novel compound heterozygous mutation in MYORG-related recessive primary familial brain calcification. CASE REPORT: We report a case of primary familial brain calcification with newly-discovered compound heterozygous mutation in the MYORG gene presenting with progressive parkinsonism, cerebellar signs, and typical diffuse brain calcifications. CONCLUSION: Clinicians should consider MYORG testing in patients who have primary brain calcifications with either a negative or recessive family history.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Encefalopatias
/
Glicosídeo Hidrolases
Limite:
Humans
Idioma:
En
Revista:
Acta Neurol Taiwan
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
Taiwan