Expanding the phenotype of COPA syndrome: a kindred with typical and atypical features

作者：Angelo M. Taveira‐DaSilva, Thomas C. Markello, David E. Kleiner, Amanda M. Jones, Catherine Groden, Ellen F. Macnamara, Tadafumi Yokoyama, William A. Gahl, Bernadette R. Gochuico, Joel Moss · 发表于：Journal of Medical Genetics · 年份：2018 · DOI：10.1136/jmedgenet-2018-105560 · 被引用次数：71 · 研究领域：Cellular transport and secretion、Histiocytic Disorders and Treatments、Peripheral Neuropathies and Disorders

BACKGROUND: Copa syndrome is a rare autosomal dominant disorder with abnormal intracellular vesicle trafficking. The objective of this work is to expand the knowledge about this disorder by delineating phenotypic features of an unreported COPA family. METHODS AND RESULTS: was identified in four members of a three-generation kindred with lung, autoimmune and malignant disease of unknown aetiology. Ages of onset were 56, 26, 16 and 1 year, with earlier age of onset in successive generations. Presenting symptoms were cough and dyspnoea. Findings included small lung cysts, follicular bronchiolitis, interstitial lung disease, neuroendocrine cell hyperplasia, rheumatoid arthritis, avascular necrosis and select abnormal autoimmune serologies. Neither alveolar haemorrhage nor glomerular disease were present. Features not previously associated with Copa syndrome included neuromyelitis optica, pulmonary carcinoid tumour, clear cell renal carcinoma, renal cysts, hepatic cysts, nephrolithiasis, pyelonephritis and meningitis. Longitudinal evaluations demonstrated slow progression of lung disease and extrapulmonary cysts. CONCLUSIONS: Worsening severity with successive generations may be observed in Copa syndrome. Extrapulmonary cysts, malignancies, autoimmune neurological disorders and infections are clinical features that may be associated with Copa syndrome. Further studies are indicated to fully define the phenotypic spectrum of this disorder.