P Hoste, J Willams, J Devriendt, H Lamont, M van der Straeten
{"title":"与皮肤白化病相关的家族性弥漫性间质性肺纤维化。两例家庭研究报告。","authors":"P Hoste, J Willams, J Devriendt, H Lamont, M van der Straeten","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Two female patients with familial diffuse fibrosing alveolitis associated with oculocutaneous albinism are presented. A family study was carried out and two other female patients with oculocutaneous albinism and pulmonary disease were detected. Clinical, radiological and histological features are highlighted and the results of treatment discussed.</p>","PeriodicalId":21508,"journal":{"name":"Scandinavian journal of respiratory diseases","volume":"60 3","pages":"128-34"},"PeriodicalIF":0.0000,"publicationDate":"1979-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Familial diffuse interstitial pulmonary fibrosis associated with oculocutaneous albinism. Report of two cases with a family study.\",\"authors\":\"P Hoste, J Willams, J Devriendt, H Lamont, M van der Straeten\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Two female patients with familial diffuse fibrosing alveolitis associated with oculocutaneous albinism are presented. A family study was carried out and two other female patients with oculocutaneous albinism and pulmonary disease were detected. Clinical, radiological and histological features are highlighted and the results of treatment discussed.</p>\",\"PeriodicalId\":21508,\"journal\":{\"name\":\"Scandinavian journal of respiratory diseases\",\"volume\":\"60 3\",\"pages\":\"128-34\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1979-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scandinavian journal of respiratory diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian journal of respiratory diseases","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Familial diffuse interstitial pulmonary fibrosis associated with oculocutaneous albinism. Report of two cases with a family study.
Two female patients with familial diffuse fibrosing alveolitis associated with oculocutaneous albinism are presented. A family study was carried out and two other female patients with oculocutaneous albinism and pulmonary disease were detected. Clinical, radiological and histological features are highlighted and the results of treatment discussed.
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