Hereditary Complete Thyroxine-Binding Globulin Deficiency: Identification by T3 Resin Uptake Test and DNA Analysis.

スポンサーリンク

概要

• 論文の詳細を見る

• Complete thyroxine-binding globulin deficiency (TBG-CD) was uncovered in a subject receiving a comprehensive health examination. The subject had an abnormally high T3 resin uptake. A family study showed that the TBG abnormality had been inherited by X-chromosome linkage. Genetic analysis revealed single nucleotide deletion, common among Japanese with TBG-CD, from the allele specific amplification of the TBG genes of the family.(Internal Medicine 32: 6-9, 1993)

• 社団法人　日本内科学会の論文

著者

• Yamamori Ikuo

  The Department Of Internal Medicine The Japanese Red Cross Nagoya First Hospital

• Takamatsu Junta

  The First Department Of Medicine Osaka Medical College

• Mori Yuichi

  The First Department Of Internal Medicine Nagoya University School Of Medicine

• KUMAHARA Yuichi

  the Sakuragaoka Hospitel Attached to the Japan Research Foundation for Chronic Diseases and Rehabilitation

• NOGUCHI Tsukasa

  the Sakuragaoka Hospitel Attached to the Japan Research Foundation for Chronic Diseases and Rehabilitation

• NAKAJIMA Tokuo

  the Sakuragaoka Hospitel Attached to the Japan Research Foundation for Chronic Diseases and Rehabilitation

関連論文

• Mass Screening for Complete Deficiency of Thyroxine-Binding Globulin in Adult Japanese by Comprehensive Health Examination
• Familial Thyroxine-Binding Globulin Deficiency Associated with Hyperthyroidism
• Prevention of Premenstrual Exacerbation of Hereditary Coproporphyria by Gonadotropin-Releasing Hormone Analogue
• Hereditary Complete Thyroxine-Binding Globulin Deficiency: Identification by T3 Resin Uptake Test and DNA Analysis.

スポンサーリンク