Birt-Hogg-Dubé Syndrome Manifesting as Spontaneous Pneumothorax: A Novel Mutation of the Folliculin Gene
The Korean Journal of Thoracic and Cardiovascular Surgery
;
: 386-390, 2017.
Article
in English
| WPRIM
| ID: wpr-139841
ABSTRACT
Birt-Hogg-Dubé syndrome (BHDS) is a rare disease with autosomal dominant inheritance that manifests through skin tumors, pulmonary cystic lesions, and renal tumors. A mutation of FLCN located on chromosome 17p11.2, which encodes a tumor-suppressor protein (folliculin), is responsible for the development of BHDS. We report the case of a patient presenting with spontaneous pneumothorax, in whom a familial genetic study revealed a novel nonsense mutation p.(Arg379*) in FLCN.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pneumothorax
/
Skin
/
Thoracoscopy
/
Wills
/
Codon, Nonsense
/
Thoracic Surgery, Video-Assisted
/
Rare Diseases
/
Estrone
/
Birt-Hogg-Dube Syndrome
Limits:
Humans
Language:
English
Journal:
The Korean Journal of Thoracic and Cardiovascular Surgery
Year:
2017
Type:
Article
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