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PedAM

Pediatric Disease Annotations & Medicines




Disease vascular disease
Phenotype C0034069|lung fibrosis
Sentences 1
PubMedID- 23697753 Assessment of the above panel of immunologic markers was performed at the following serial time points: 1) at time of diagnosis as a part of routine work-up in order to exclude collagen vascular diseases as a cause of lung fibrosis, and 2) at regular follow-up every 6 months or earlier than 6 months if clinical signs compatible with autoimmune disease (arthralgia, muscle weakness, dysphagia, raynaud’s phenomenon, photosensitivity) or disease exacerbation (dyspnea deterioration, hemoptysis, hematuria) emerged.

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