A interstial lung disease characterized by the presence of persistent or intermittent tachypnea (usually noticed in neonatal period or after an acute infection for the first time in first months of life), crackles in 86 %, retractions in 82%, failure to thrive in 66%, chest wall abnormalities in 22% and hypoxemia or desaturation in 88%.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
pulmonary interstitial glycogenosis
MONDO:0016321
neuroendocrine cell hyperplasia of infancy
MONDO:0016322
chronic pneumonitis of infancy
MONDO:0019621
persistent tachypnoe of infancy, aberrant
MONDO:0800110
persistent tachypnoe of infancy, usual
MONDO:0800111
cellular interstitial pneumonitis
MONDO:0800121