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The Assessment of a Patient with Ataxia-Telangiectasia (A-T): A Case Report Study
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  • Marziyeh Heidarzadeh,
  • Reza ArefNezhad,
  • Javad Fathgharib,
  • Asghar Aghamohammadi ,
  • Hossein Motedayyen
Marziyeh Heidarzadeh
Kashan University of Medical Sciences
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Reza ArefNezhad
Shiraz University of Medical Sciences
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Javad Fathgharib
Kashan University of Medical Sciences
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Asghar Aghamohammadi
Tehran University of Medical Sciences
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Hossein Motedayyen
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Peer review status:UNDER REVIEW

11 Apr 2020Submitted to Clinical Case Reports
18 Apr 2020Assigned to Editor
18 Apr 2020Submission Checks Completed
01 Jul 2020Reviewer(s) Assigned
27 Jul 2020Review(s) Completed, Editorial Evaluation Pending

Abstract

Ataxia-telangiectasia (A-T) is a multi-system disorder, resulted from the mutation in the ATM gene. Its mortality is largely related to some other disorders. Therefore, the management of its complications significantly improves patient quality of life. We studied a pediatric patient with A-T who one of his relatives had A-T.