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  2. Childhood interstitial lung disease - Wikipedia

    en.wikipedia.org/wiki/Childhood_interstitial...

    Childhood interstitial lung disease, sometimes abbreviated as ChILD, is a family of rare chronic and complex disorders that affect the lungs of children. [1] In the lungs, these disorders affect the interstitium, which is the space around the alveoli. The alveoli are the air sacs of the lungs. [2]

  3. Alveolar capillary dysplasia - Wikipedia

    en.wikipedia.org/wiki/Alveolar_capillary_dysplasia

    ACD is a rare disease. As of 2011, about 100 cases had been reported. It is likely an under-recognized cause of death shortly after birth because diagnosis requires microscopic examination of lung tissue or specialized genetic testing, or death can be attributed to severe heart or intestinal congenital abnormalities which frequently occur in ACD.

  4. Pulmonary alveolar microlithiasis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_alveolar_micro...

    Pulmonary Alveolar Microlithiasis patients, families, and caregivers are encouraged to join the NIH Rare Lung Diseases Consortium Contact Registry. This is a privacy protected site that provides up-to-date information for individuals interested in the latest scientific news, trials, and treatments related to rare lung diseases. [citation needed]

  5. Swyer–James syndrome - Wikipedia

    en.wikipedia.org/wiki/Swyer–James_syndrome

    Rare [2] Swyer–James syndrome ( SJS ), also called Swyer–James–MacLeod syndrome , is a rare disease of the lungs , characterized by a small lung or part of lung. [ 1 ] Typical symptoms are of recurrent respiratory tract infections , but some have no symptoms.

  6. Pulmonary alveolar proteinosis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_alveolar_proteinosis

    Pulmonary alveolar proteinosis (PAP) is a rare lung disorder characterized by an abnormal accumulation of surfactant-derived lipoprotein compounds within the alveoli of the lung. The accumulated substances interfere with the normal gas exchange and expansion of the lungs, ultimately leading to difficulty breathing and a predisposition to ...

  7. Primary ciliary dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Primary_ciliary_dyskinesia

    Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive genetic ciliopathy, that causes defects in the action of cilia lining the upper and lower respiratory tract, sinuses, Eustachian tube, middle ear, fallopian tube, and flagella of sperm cells.

  8. Birt–Hogg–Dubé syndrome - Wikipedia

    en.wikipedia.org/wiki/Birt–Hogg–Dubé_syndrome

    Birt-Hogg-Dubé Syndrome patients, families, and caregivers are encouraged to join the NIH Rare Lung Diseases Consortium Contact Registry. This is a privacy-protected site that provides up-to-date information for individuals interested in the latest scientific news, trials, and treatments related to rare lung diseases.

  9. Lymphangioleiomyomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangioleiomyomatosis

    Video-assisted thoracoscopic lung biopsy is the most definitive technique, but transbronchial biopsy has a yield of over 50% and can also be effective. [82] [83] The safety of the latter procedure in patients with diffuse cystic disease and the profusion of cystic change that predicts an informative biopsy are incompletely understood, however ...