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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

Corresponding Author:[email protected]

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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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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.

Peer review status:ACCEPTED

11 Apr 2020Submitted to Clinical Case Reports
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18 Apr 2020Submission Checks Completed
18 Apr 2020Assigned to Editor
01 Jul 2020Reviewer(s) Assigned
27 Jul 2020Review(s) Completed, Editorial Evaluation Pending
06 Oct 2020Editorial Decision: Revise Minor
24 Oct 20201st Revision Received
26 Oct 2020Submission Checks Completed
26 Oct 2020Assigned to Editor
26 Oct 2020Review(s) Completed, Editorial Evaluation Pending
05 Nov 2020Editorial Decision: Accept