pulmonary fibrosis - vertaling naar arabisch
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pulmonary fibrosis - vertaling naar arabisch


pulmonary fibrosis         
‎ تَلَيُّفٌ رِئَوِيّ‎
fibrosing alveolitis         
  • Clubbing of the fingers in idiopathic pulmonary fibrosis
  • archive-date=27 February 2019 }}</ref>
  • alt=Pathobiology of IPF
  • Classification of IIPs.<ref name="ATS/ERS"/>
  • High-resolution computed tomography scans of the chest of a patient with IPF. The main features are of a peripheral, predominantly basal pattern of coarse reticulation with honeycombing
  • Photomicrograph of the histopathological appearances of usual interstitial pneumonia. High-power magnification (on the right) shows a focus of fibroblastic proliferation, close to an area of fibrosis within which a mild, non-specific, chronic inflammatory cell infiltrate can be observed. In the subpleural space, a typical honeycombing aspect can be recognized.
  • A chest radiograph of a patient with IPF. Note the small lung fields and peripheral pattern of reticulonodular opacification.
CHRONIC, IRREVERSIBLE AND ULTIMATELY FATAL DISEASE CHARACTERIZED BY A PROGRESSIVE DECLINE IN LUNG FUNCTION
Cryptogenic fibrosing alveolitis; Idiopathic Pulmonary Fibrosis; Fibrosing Alveolitis; Idiopathic fibrotizing alveolitis; Idiopathic fibrosing alveolitis; Fibrosing alveolitis
‎ الْتِهابُ الأسْنَاخِ الرِّئَوِيَّة المُلَيِّف‎
fibrocystic disease of the pancreas         
  • Health problems associated with cystic fibrosis
  • The CFTR protein is a channel protein that controls the flow of H<sub>2</sub>O and Cl<sup>−</sup> ions in and out of cells inside the lungs. When the CFTR protein is working correctly, ions freely flow in and out of the cells. However, when the CFTR protein is malfunctioning, these ions cannot flow out of the cell due to a blocked channel. This causes cystic fibrosis, characterized by the buildup of thick mucus in the lungs.
  • The location of the ''CFTR'' gene on chromosome 7
  • Respiratory infections in CF vary according to age.<br><br>Green = ''[[Pseudomonas aeruginosa]]''<br>Brown = ''[[Staphylococcus aureus]]''<br>Blue = ''[[Haemophilus influenzae]]''<br>Red = ''[[Burkholderia cepacia]]'' complex
  • [[Dorothy Hansine Andersen]] first described cystic fibrosis in 1938.
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  • Intracytoplasmic sperm injection can be used to provide fertility for men with cystic fibrosis.
AUTOSOMAL RECESSIVE DISEASE CHARACTERIZED BY THE BUILDUP OF MUCUS
Mucoviscidosis; Cistic fibrosis; Cystic Fiborsis; Cystic fibrosis allele; Cystic fibrose; Mucoviscidose; Viscoidosis; Mucuviscoidosis; Mucoviscoidosis; Mucoviscidopsis; Fibrocystic disease of the pancreas; Cystic Fibrosis; Cyctic fibrosis; Cystic Fibrosis (CF); History of Cystic fibrosis; Gene therapy for cystic fibrosis; Treatment of cystic fibrosis
‎ الداءُ الكيسِيُّ اللِّيفِيُّ في البنكرياس‎

Definitie

cystic fibrosis
Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult.
N-UNCOUNT

Wikipedia

Pulmonary fibrosis
Pulmonary fibrosis is a condition in which the lungs become scarred over time. Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.
Voorbeelden uit tekstcorpus voor pulmonary fibrosis
1. He had diabetes and the incurable lung disease pulmonary fibrosis.
2. He was diagnosed with pulmonary fibrosis, a rare disease that is poorly understood.
3. Judge, who suffered from pulmonary fibrosis, died at Chandler Regional Hospital in Chandler, Ariz., said his sons, Thomas and Patrick.
4. The cause of death, she said, was idiopathic pulmonary fibrosis, a progressive and a fatal scarring of the lungs.
5. He died of complications from pulmonary fibrosis, a progressive scarring of the lungs he had been diagnosed with last autumn, son–in–law Chris Turner said.