Disorders of surfactant metabolism (Q42941): Difference between revisions
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Doença intersticial pulmonar primária específica da infância devida a anomalias da proteína do surfactante pulmonar é um grupo de doenças intersticiais pulmonares (DIP) induzidas por mutações genéticas interferindo na função do surfactante e na troca gasosa no pulmão. Os transtornos causados per estas mutações afetam bebês nascidos a termo e crianças mais velhas, e exibem considerável sobreposição em sua apresentação clínica e histológica. | |||
| description / en | description / en | ||
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies is a group of interstitial lung diseases (ILD) induced by genetic mutations disrupting surfactant function and gas exchange in the lung. The disorders caused by these mutations affect full-term infants and older children and exhibit considerable overlap in their clinical and histologic presentation | |||
Revision as of 09:42, 13 August 2026
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies is a group of interstitial lung diseases (ILD) induced by genetic mutations disrupting surfactant function and gas exchange in the lung. The disorders caused by these mutations affect full-term infants and older children and exhibit considerable overlap in their clinical and histologic presentation
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | CB04.2 |
||
| English | Disorders of surfactant metabolism |
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies is a group of interstitial lung diseases (ILD) induced by genetic mutations disrupting surfactant function and gas exchange in the lung. The disorders caused by these mutations affect full-term infants and older children and exhibit considerable overlap in their clinical and histologic presentation |
