1 / 38

Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis

Pulmonary alveolar microlithiasis (PAM) is a rare, most probably autosomal recessive condition, characterised by concretions of calcium phosphate deposits in the pulmonary alveoli. Friedrich was the first to observe and describe the disease during an otopsy, in 1856. Harbitz reported the first case

meryl
Télécharger la présentation

Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

    1. Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis 1. Department of Molecular Biology and Genetics, Bogazici University, Istanbul 2. Department of Chest Diseases, Faculty of Medicine, Dicle University,Diyarbakir, 3. Yedikule Hospital for Pulmonary Diseases, Istanbul 4. Department of Pediatric Pulmonary Diseases, Faculty of Medicine, Hacettepe University, Ankara 5. Sureyyapasa Training and Research Hospital for Pulmonary and Cardiovascular Diseases, Istanbul 6. Department of Chest Diseases, Faculty of Medicine, Inonu University, Malatya

More Related