
The interstitial lung diseases (ILDs), or diffuse parenchymal lung diseases, are a heterogeneous collection of more than 100 different pulmonary disorders that affect the tissue and spaces surrounding the alveoli. Patients affected by ILD usually present with shortness of breath or cough; for many, there is evidence of pulmonary restriction, decreased diffusion capacity, and radiographic appearance of alveolar and/or reticulonodular infiltrates. This article reviews the inherited ILDs, with a focus on the diseases that may be seen by pulmonologists caring for adult patients. The authors conclude by briefly discussing the utility of genetic testing in this population.
Adult, Lung Diseases, Heterozygote, Pulmonary Surfactant-Associated Protein B, Pulmonary Fibrosis, Genetic Diseases, Inborn, Calcinosis, Pneumothorax, Genetic Diseases, X-Linked, Pulmonary Alveolar Proteinosis, Pulmonary Surfactant-Associated Protein C, Kidney Neoplasms, Pedigree, Birt-Hogg-Dube Syndrome, INDEL Mutation, Proto-Oncogene Proteins, Mutation, Humans, Female, Lung Diseases, Interstitial
Adult, Lung Diseases, Heterozygote, Pulmonary Surfactant-Associated Protein B, Pulmonary Fibrosis, Genetic Diseases, Inborn, Calcinosis, Pneumothorax, Genetic Diseases, X-Linked, Pulmonary Alveolar Proteinosis, Pulmonary Surfactant-Associated Protein C, Kidney Neoplasms, Pedigree, Birt-Hogg-Dube Syndrome, INDEL Mutation, Proto-Oncogene Proteins, Mutation, Humans, Female, Lung Diseases, Interstitial
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