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Primary Familial Brain Calcification Caused by a Novel Compound Heterozygous Mutation in the MYORG Gene.
Tsai, Ming-Chen; Lee, Jiunn-Tay; Sung, Yueh-Feng; Yang, Fu-Chi.
Afiliação
  • Tsai MC; Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Lee JT; Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Sung YF; Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Yang FC; Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
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
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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