Primary Spontaneous Pneumothorax
What's New
Last Posted: Mar 03, 2023
- Familial spontaneous pneumothorax: importance of screening for Birt-Hogg-Dubé syndrome.
Liu Yanguo, et al. European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2019 0 (1) 39-45 - Genetic insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations at FLCN.
Ray Anindita, et al. Orphanet journal of rare diseases 2022 0 (1) 176 - Association of Alpha 1-antitrypsin Deficiency and Genetic Predisposition in Primary Spontaneous Pneumothorax.
Sahin Taner, et al. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2021 7 (7) 775-779 - A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
Zhang Xinxin et al. Respiratory research 2016 May 17(1) 64 - Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.
Sousa Inês, et al. PloS one 2016 0 (5) e0156103 - FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax.
Ding Yibing, et al. American journal of medical genetics. Part A 2015 5 (5) 1125-33 - Primary spontaneous pneumothorax
From NCATS Genetic and Rare Diseases Information Center - Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Ren H-Z, et al. Clinical genetics 2008 8 (2) 178-83
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: