论文部分内容阅读
患者生长发育迟缓、身材矮小、染色体检查异常,染色体核型46,Xi(Xq)。FPG 7.68mmol/L↑,2h PG15.57mmol/L↑。C-P水平低下。(谷氨酸脱羧酶抗体)GAD-AB 108.70 U/ml↑,(酪氨酸磷酸化酶抗体)IA2-AB0.00 U/ml。超敏TSH 3.97IU/L,抗甲状腺球蛋白抗体(TGAb)691.10KIU/L↑,抗甲状腺过氧化物抗体(TPOAb)600.0KIU/L↑,甲状腺球蛋白0.040ug/L↓。诊断turner综合征合并1型糖尿病及桥本氏甲状腺炎。
Patients with growth retardation, short stature, chromosomal abnormalities, chromosome karyotype 46, Xi (Xq). FPG 7.68 mmol / L ↑, 2h PG 15.57 mmol / L ↑. C-P level is low. (Glutamic acid decarboxylase antibody) GAD-AB 108.70 U / ml ↑, (tyrosine phosphorylase antibody) IA2-AB 0.00 U / ml. Hypercholesterolemic TSH 3.97IU / L, anti-thyroglobulin antibody (TGAb) 691.10KIU / L ↑, anti-thyroid peroxide antibody (TPOAb) 600.0KIU / L ↑, thyroglobulin 0.040ug / L ↓. Diagnosis of turner syndrome with type 1 diabetes and Hashimoto’s thyroiditis.