A 10-Year-Old Boy With Ataxia-Telangiectasia: A Rare Case Report From Yemen

This case emphasizes the importance of considering A-T in children with recurrent chest infections and neurological symptoms. Early diagnosis facilitates timely supportive care, including immunization, pulmonary management, malignancy surveillance, and genetic counseling for families.

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Publication Details

Journal
Clinical Medicine Insights Case Reports
Published
2025-12-01
DOI
https://doi.org/10.1177/11795476251408138
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

A 10-Year-Old Boy With Ataxia-Telangiectasia: A Rare Case Report From Yemen

Anas Saeed Abdulmalek Al-Kubati, Bilal Sleiay, Maher Muneer, Betoul Mohammad Alhofari et al.
Clinical Medicine Insights Case Reports
DNA Repair Mechanisms
article

A 10-Year-Old Boy With Ataxia-Telangiectasia: A Rare Case Report From Yemen

Anas Saeed Abdulmalek Al-Kubati, Bilal Sleiay, Maher Muneer, Betoul Mohammad Alhofari, Laila Salama Daas, Majed Shallan, Laila Albaseer, Asma’a Al-Ghashm, Abdullah Alkubati
article en

Abstract

This case emphasizes the importance of considering A-T in children with recurrent chest infections and neurological symptoms. Early diagnosis facilitates timely supportive care, including immunization, pulmonary management, malignancy surveillance, and genetic counseling for families.

Clinical Medicine Insights Case ReportsVol. 18
University of Science and Technology (YE), Sana'a University (YE), University of Kalamoon (SY), Al-Razi University (YE), Damascus University (SY)
Good health and well-being
Openalex Percentile: Top 37%
DNA Repair Mechanisms
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