Abstract
Ataxia telangiectasia (A-T) is a rare, progressive, multisystem disease that has a large number of complex and diverse manifestations which vary with age. Patients with A-T die prematurely with the leading causes of death being respiratory diseases and cancer. Respiratory manifestations include immune dysfunction leading to recurrent upper and lower respiratory infections; aspiration resulting from dysfunctional swallowing due to neurodegenerative deficits; inefficient cough; and interstitial lung disease/pulmonary fibrosis. Malnutrition is a significant comorbidity. The increased radiosensitivity and increased risk of cancer should be borne in mind when requesting radiological investigations. Aggressive proactive monitoring and treatment of these various aspects of lung disease under multidisciplinary expertise in the experience of national multidisciplinary clinics internationally forms the basis of this statement on the management of lung disease in A-T. Neurological management is outwith the scope of this document.
| Original language | English |
|---|---|
| Pages (from-to) | 565-581 |
| Number of pages | 17 |
| Journal | European respiratory review : an official journal of the European Respiratory Society |
| Volume | 24 |
| Issue number | 138 |
| Early online date | 30 Nov 2015 |
| DOIs | |
| Publication status | Published - Dec 2015 |
Bibliographical note
ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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