Jo Wakako, Ishizu Katsura, Fujieda Kenji, Tajima Toshihiro
Department of Pediatrics, Hokkaido University School of Medicine, N15, W7, Sapporo, Hokkaido 060-8638, Japan.
J Thyroid Res. 2010;2010:619013. doi: 10.4061/2010/619013. Epub 2009 Dec 9.
Loss-of-function mutations of the PAX8 gene are considered to mainly cause congenital hypothyroidism (CH) due to thyroid hypoplasia. However, some patients with PAX8 mutation have demonstrated a normal-sized thyroid gland. Here we report a CH patient caused by a PAX8 mutation, which manifested as iodide transport defect (ITD). Hypothyroidism was detected by neonatal screening and L-thyroxine replacement was started immediately. Although (123)I scintigraphy at 5 years of age showed that the thyroid gland was in the normal position and of small size, his iodide trapping was low. The ratio of the saliva/plasma radioactive iodide was low. He did not have goiter; however laboratory findings suggested that he had partial ITD. Gene analyses showed that the sodium/iodide symporter (NIS) gene was normal; instead, a mutation in the PAX8 gene causing R31H substitution was identified. The present report demonstrates that individuals with defective PAX8 can have partial ITD, and thus genetic analysis is useful for differential diagnosis.
PAX8基因功能丧失突变被认为主要因甲状腺发育不全导致先天性甲状腺功能减退症(CH)。然而,一些携带PAX8突变的患者甲状腺大小正常。在此,我们报告1例由PAX8突变引起的CH患者,其表现为碘转运缺陷(ITD)。通过新生儿筛查发现甲状腺功能减退症,并立即开始左旋甲状腺素替代治疗。尽管5岁时的(123)I闪烁扫描显示甲状腺位置正常但体积较小,但其碘摄取率较低。唾液/血浆放射性碘的比率较低。他没有甲状腺肿;然而实验室检查结果提示他存在部分ITD。基因分析显示钠/碘同向转运体(NIS)基因正常;相反,鉴定出PAX8基因发生导致R31H替代的突变。本报告表明,PAX8缺陷的个体可出现部分ITD,因此基因分析有助于鉴别诊断。