ORPHA:264675
Hereditary pulmonary alveolar proteinosis
Also called Congenital PAP, Congenital pulmonary alveolar proteinosis
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adolescent, Adult, Childhood, Elderly, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:264675 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Abnormal circulating protein level
- Failure to thrive in infancy
- Restrictive ventilatory defect
- Respiratory distress
- Respiratory failure requiring assisted ventilation
- Hypoxemia