Defective Deiodination of <SUP>131</SUP>I-Labeled L-Diiodotyrosine in a Family with Cases of Euthyroid Goiter and Hyperthyroidism
スポンサーリンク
概要
- 論文の詳細を見る
The <SUP>131</SUP>I-DIT deiodination test revealed a defect of DIT dehalogenase as the cause of euthyroid goiter in a 9 year old boy. Among 21 of his pedigree, 13 had a similar defect of DIT dehalogenase. Four patients with euthyroid goiter, 1 patient with hyperthyroidism, and 8 non-goitrous euthyroid subjects were found among these 13 relatives. No defect of MIT deiodination was found in any of these cases. In this family, the mode of inheritance of the defect of DIT dehalogenase appeared to be autosomal dominant.
- 社団法人 日本内分泌学会の論文
著者
-
NAKAJIMA Hironori
Department of Mechanical Engineering, Kyushu University
-
Niimi Hiroo
Department Of Pediatrics Chiba University School Of Medicine
-
FUJIMORI MUNENORI
Department of Pediatrics, Chiba University School of Medicine
関連論文
- Expression of tumor necrosis factor-α protein in the myocardium in fatal myocarditis
- Influences of Microporous Layer Design Parameters for Gas Diffusion Layer on Permeability and PEFC Performance
- Increased expression of α4β7 integrin on food allergen-stimulated CD4^+ T cells in active food allergic enterocolitis
- Clinical Utility of Thyroid Ultrasonography in the Diagnosis of Congenital Hypothyroidism
- Abnormal DNA synthesis induction in X-ray-irradiated Gorlin fibroblast cells
- Intradural spinal meningioma in a 5-year-old female
- Direct demonstration of humorally mediated inhibition of the transcription of phosphate transporter in XLH patients
- Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
- Polycyclic Aromatic Hydrocarbon Increases mRNA Level for Interleukin 1 Beta in Human Fibroblast-Like Synoviocyte Line via Aryl Hydrocarbon Receptor (Analytical Biochemistry)
- Fulminant ulcerative colitis associated with both masseter muscle myositis and immunoglobulin M nephropathy
- Characteristics of β-Lactamase - Producing and Amoxicillin-Clavulanate - Resistant Strains of Haemophilus influenzae Isolated from Pediatric Patients
- Jansen-type Metaphyseal Chondrodysplasia : Analysis of PTH/PTH-related Protein Receptor Messenger RNA by the Reverse Transcriptase-Polymerase Chain Method
- Early Detection of Infants with Hypophosphatemic Vitamin D Resistant Rickets (HDRR)
- Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cells
- A case of epilepsia partialis continua associated with hemimegalencephaly
- CATCH22 syndrome with qastroesophageal reflux
- Clinical and MRI findings in a case of D-2-hydroxyglutaric aciduria
- -137- KAWASAKI DISEASE WITH THROMBOCYTOPENIA : Congenital Heart Disease, Kawasaki Disease : FREE COMMUNICATIONS(I) : PROCEEDINGS OF THE 51th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- Evaluation of L-Thyroxine Requirement in Treatment of Congenital Hypothyroidism
- A SIMPLIFIED METHOD FOR DETERMINATION OF BLOOD CORTICOIDS USING IN VITRO RESIN SPONGE UPTAKE OF 3H-PREDNISOLONE
- Defective Deiodination of 131I-Labeled L-Diiodotyrosine in a Family with Cases of Euthyroid Goiter and Hyperthyroidism
- Familial Thyroxine-Binding Globulin Deficiency in a Patient with Congenital Hypothyroidism
- Significant Fluctuation of Thyroid Function in Children with Chronic Lymphocytic Thyroiditis
- High Incidence of Chronic Lymphocytic Thyroiditis in Apparently Healthy School Children: Epidemiological and Clinical Study
- STUDIES ON THE PATHOGENESIS OF HYPOPHOSPHATEMIC VITAMIN D REFRACTORY RICKETS OF THE SIMPLE TYPE OR PHOSPHATDIABETES