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Image of Dilemma of presymptomatic testing in children with history of late onset neurodegenerative spinocerebellar ataxia in Indonesia

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Dilemma of presymptomatic testing in children with history of late onset neurodegenerative spinocerebellar ataxia in Indonesia

Nydia Rena Benita Sihombing - Personal Name; Tri Indah Winarni - Personal Name; Maria Belladonna - Personal Name; Annastasia Ediati - Personal Name; Sultana MH Faradz - Personal Name;

Background: Spinocerebellar ataxia (SCA) is a late onset neurodegenerative disorder in which coordination and balance are affected. Although many international guidelines have been established regarding presymptomatic testing, it is still a grey area in Indonesia. We report two large families with advanced stages of SCA who underwent presymptomatic genetic testing in children along counseling process. Case presentation: Thorough examination was performed, including pedigree construction, physical and neurological examination, gene mutation analyses for patients, and presymptomatic testing for family members, including children. SCA3/MJD1gene mutation analysis was done in both cases, and a full penetrance CAG repeat expansion was found in both affected patients. Two different outcomes were observed in the offspring, who were both children. The risk and consequences of positive results had been explained in a counseling session to family members, who decided to keep the information until the child would have reached legally adult age of 18. Conclusions: In developing countries such as Indonesia, problems arose due to ethical issues, knowledge of genetic diseases, and inaccessible molecular diagnostics. Culture, religion and tribe diversities may create additional challenges. These cases emphasize the need for careful consideration of presymptomatic testing in children, especially in complicated situations where psychological and ethical issues should be addressed. Keywords:Case Report; Genetic Counseling; Presymptomatic Testing; Spinocerebellar Ataxia; Indonesia


Availability
#
Perpustakaan RSUP Dr. Kariadi Semarang 616.834 NYD d
P00425S
Available
Detail Information
Series Title
-
Call Number
616.834 NYD d
Publisher
Semarang : Journal of Biomedicine and Translational Research., 2022
Collation
-
Language
English
ISBN/ISSN
-
Classification
616.834
Content Type
-
Media Type
-
Carrier Type
-
Edition
-
Subject(s)
Genetic Testing
Spinocerebellar Ataxias
Neurodegenerative Diseases
Specific Detail Info
-
Statement of Responsibility
Nydia Rena Benita Sihombing
Viewer
282
Other Information
Tanggal Pelaksanaan - Dari
2024-12-31
Tanggal Pelaksanaan - Sampai
2024-12-31
Akreditasi
Tidak
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  • Dilemma of presymptomatic testing in children with history of late onset neurodegenerative spinocerebellar ataxia in Indonesia
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