Graham J M, Saunders R, Fratkin J, Spiegel P, Harris M, Klein R Z
Department of Maternal and Child Health, Dartmouth Hitchcock Medical Center, Hanover, New Hampshire 03756.
Am J Med Genet Suppl. 1986;2:53-63. doi: 10.1002/ajmg.1320250609.
We report on three infants with hand anomalies and congenital hypopituitarism. In two of the cases, a hypothalamic tumor was found; the third infant died without postmortem brain studies. Family history in the first case suggested possible familial recurrence; the mother's sister had died at 17 hr of age with polydactyly, microglossia, and flat nasal bridge (no autopsy done). Our second case was born by cesarean section after a pregnancy complicated by extremely low maternal estriols. At birth, hypopituitarism was diagnosed, a cranial CT scan was read as normal, and hormonal replacement was begun with thyroxine, hydrocortisone, and growth hormone. At 11.5 mo of age she developed seizures; and a repeat CT scan showed a mass extending beneath the hypothalamus. This tumor was removed surgically at 12 mo, the first successful treatment of this disorder. Our third possible case had a bifid epiglottis, hypopituitarism, and hand anomalies. A CT scan at birth failed to reveal a mass in the hypothalamus. This child died from complications of untreated hypopituitarism, and no neuropathology studies were done. These three cases were conceived between March 10th and April 17th in three different years in three geographically contiguous counties of Vermont. Clustering in time and space and possible familial recurrence, in one of these cases, suggest a possible gene/environment interaction.
我们报告了三例患有手部异常和先天性垂体功能减退的婴儿。其中两例发现有下丘脑肿瘤;第三例婴儿未进行尸检脑研究就死亡了。第一例的家族史提示可能存在家族性复发;母亲的妹妹在17小时龄时死于多指畸形、小舌症和扁平鼻梁(未进行尸检)。我们的第二例婴儿是在母亲雌三醇水平极低的复杂孕期后通过剖宫产出生的。出生时诊断为垂体功能减退,头颅CT扫描结果显示正常,遂开始用甲状腺素、氢化可的松和生长激素进行激素替代治疗。在11.5月龄时她出现癫痫发作;复查CT扫描显示有一个肿块延伸至下丘脑下方。该肿瘤在12月龄时通过手术切除,这是对该疾病的首次成功治疗。我们的第三例可能病例有会厌裂、垂体功能减退和手部异常。出生时的CT扫描未发现下丘脑有肿块。这个孩子死于未经治疗的垂体功能减退的并发症,未进行神经病理学研究。这三例病例分别于不同年份的3月10日至4月17日期间在佛蒙特州三个地理上相邻的县受孕。其中一例在时间和空间上的聚集以及可能的家族性复发提示可能存在基因/环境相互作用。