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Birt-Hogg-Dube syndrome incidentally diagnosed during asthma management
Allergy, Asthma & Respiratory Disease ; : 232-235, 2015.
Article in Korean | WPRIM | ID: wpr-102765
ABSTRACT
Birt-Hogg-Dube (BHD) syndrome is an autosomal dominant hereditary disorder characterized by 3 clinical manifestations, including skin fibrofolliculomas, multiple pulmonary cysts with or without spontaneous pneumothorax, and spontaneous renal tumor. A 60-year-old Korean male who had suffered from bronchial asthma incidentally diagnosed with multiple pulmonary cysts by computed tomography during a regular follow-up. Genetic studies revealed folliculin gene mutation that was a confirmative finding of BHD syndrome. Although this case showed no cutaneous manifestations or renal abnormality, genetic studies of his family and regular follow-up are recommended.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pneumothorax / Asthma / Skin / Follow-Up Studies / Estrone / Birt-Hogg-Dube Syndrome / Kidney Neoplasms Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans / Male Language: Korean Journal: Allergy, Asthma & Respiratory Disease Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pneumothorax / Asthma / Skin / Follow-Up Studies / Estrone / Birt-Hogg-Dube Syndrome / Kidney Neoplasms Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans / Male Language: Korean Journal: Allergy, Asthma & Respiratory Disease Year: 2015 Type: Article