Department of Pediatrics, The University of Texas Health Science Center, Houston, 6431 Fannin, MSB 3.122, Houston, TX 77030, USA.
Pituitary. 2012 Dec;15 Suppl 1:S1-5. doi: 10.1007/s11102-010-0230-y.
A 3-year 5-month-old boy was seen for second opinion regarding polydipsia and polyuria. Previously, a diagnosis of primary polydipsia was made after normal urine concentration after overnight water deprivation testing. The boy's father, paternal grandfather, and paternal aunt had diabetes insipidus treated with desmopressin acetate. Based on this young boy's symptoms, ability to concentrate urine after informal overnight water deprivation, and family history of diabetes insipidus, we performed AVP gene mutation testing. Analysis of the AVP gene revealed a novel mutation G54E that changes a normal glycine to glutamic acid, caused by a guanine to adenine change at nucleotide g.1537 (exon 2) of the AVP gene. Commonly, patients with familial neurohypophyseal diabetes insipidus (FNHDI) present within the first 6 years of life with progressively worsening polyuria and compensatory polydipsia. Since these patients have progressive loss of arginine vasopressin (AVP), they may initially respond normally to water deprivation testing and have normal pituitary findings on brain MRI. Genetic testing may be helpful in these patients, as well as preemptively diagnosing those with a mutation, thereby avoiding unnecessary surveillance of those unaffected.
一名 3 岁 5 个月大的男孩因多饮多尿前来就诊,寻求第二诊疗意见。此前,经过 overnight water deprivation testing(夜间限水试验),其尿液浓缩功能正常,因此被诊断为原发性多饮症。男孩的父亲、祖父和姑姑均患有尿崩症,使用醋酸去氨加压素进行治疗。根据这个小男孩的症状、夜间限水试验后浓缩尿液的能力,以及家族性尿崩症病史,我们进行了 AVP 基因突变检测。AVP 基因分析显示一种新的突变 G54E,导致正常甘氨酸突变为谷氨酸,是由鸟嘌呤到腺嘌呤的变化引起的,位于 AVP 基因的核苷酸 g.1537(外显子 2)。通常,家族性神经垂体性尿崩症(FNHDI)患者在生命的前 6 年内会出现逐渐加重的多尿和代偿性多饮。由于这些患者逐渐失去精氨酸加压素(AVP),他们可能最初对限水试验有正常反应,且脑 MRI 上的垂体表现正常。遗传检测可能对这些患者有帮助,也有助于对突变患者进行预防性诊断,从而避免对未受影响的患者进行不必要的监测。