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.
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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
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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

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