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Figure 1 | Journal of Medical Case Reports

Figure 1

From: A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case report

Figure 1

Pulmonary function testing data. A. Acquired at 2 years of age using the raised volume rapid thoracoabdominal compression technique along with whole body plethysmography. Normative data by Castile et al. and Jones et al. [4, 6]. B. Acquired at 4 years of age using classical spirometry and whole body plethysmography. FVC- Forced vital capacity; FEV0.5 - Forced expiratory volume in 0.5 second; FEF25-75 - Forced expiratory flow between 25 and 75% of the FVC; FEF75 - Forced expiratory flow at 75% of the FVC; FEF85 - Forced expiratory flow at 85% of the FVC; TLC- Total lung capacity; FRC- Functional residual capacity; RV- Residual volume; FEV1 – Forced expiratory volume in 1 second; VC- Vital capacity.

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