Powell B R, Buist N R
Department of Pediatrics, Doernbecher Memorial Hospital for Children, Oregon Health Sciences University, Portland 97201.
Clin Pediatr (Phila). 1990 Apr;29(4):241-3. doi: 10.1177/000992289002900409.
Familial hypocalciuric hypercalcemia (FHH) is a benign autosomal dominant disorder. Infants affected with FHH however, born to unaffected mothers may develop life-threatening autonomous hyperparathyroidism, the mechanism of which is not clearly understood. There is little information recorded in the literature regarding the opposite scenario, i.e., unaffected infants born to affected mothers. Because fetal parathyroid suppression presumably occurs secondary to high maternal calciums, neonatal hypocalcemia would be expected. The authors present a case of an infant with the latter circumstances who presents with late onset, life-threatening hypocalcemia secondary to relative hypoparathyroidism. The authors explored the possibility that vitamin D deficiency and/or acute environmental stress facilitated the decompensation. The patient required therapy for 2 months.
家族性低钙尿性高钙血症(FHH)是一种良性常染色体显性疾病。然而,患有FHH的婴儿,其母亲未患病,这些婴儿可能会发展为危及生命的自主性甲状旁腺功能亢进,其发病机制尚不清楚。关于相反情况,即患病母亲所生的未患病婴儿,文献中记载的信息很少。由于胎儿甲状旁腺抑制可能继发于母亲高钙血症,预计会出现新生儿低钙血症。作者报告了一例处于后一种情况的婴儿,该婴儿因相对甲状旁腺功能减退出现迟发性、危及生命的低钙血症。作者探讨了维生素D缺乏和/或急性环境应激促成失代偿的可能性。该患者需要接受2个月的治疗。