Diagnosis of a patient with Spinocerebellar ataxia type 29 due to a novel variant of ITPR1 gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 76-80, 2023.
Article
ي Zh
| WPRIM
| ID: wpr-970882
المكتبة المسؤولة:
WPRO
ABSTRACT
OBJECTIVE@#To explore the clinical and genetic characteristics of a child with spinocerebellar ataxia type 29 (SCA29) due to novel variant of the inositol 1,4,5-trisphosphate receptor type 1 (ITPR1) gene.@*METHODS@#The child was subjected high-throughput sequencing, and candidate variant was verified by Sanger sequencing of his family members.@*RESULTS@#The child was found to harbor a c.800C>T (p.T267M) variant of the ITPR1 gene, which was not found in his parents and their fetus. The variant has occurred in a hotspot of the ITPR1 gene variants and was unreported before in China. Based on his clinical and genetic characteristics, the child was diagnosed with SCA29.@*CONCLUSION@#The novel heterozygous c.800C>T (p.T267M) of the ITPR1 gene probably underlay the SCA29 in this child.
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Family
/
Spinocerebellar Degenerations
/
Spinocerebellar Ataxias
/
Inositol 1,4,5-Trisphosphate Receptors
/
Mutation
المحددات:
Child
/
Humans
اللغة:
Zh
مجلة:
Chinese Journal of Medical Genetics
السنة:
2023
نوع:
Article