Familial diffuse interstitial pulmonary fibrosis associated with oculocutaneous albinism. Report of two cases with a family study.

Abstract

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.