Nguyen Minh, Litra Florentina, Kamil Ammar, Ergun-Longmire Berrin
Internal Medicine/Pediatrics, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, USA.
Pediatrics, University of Florida, Pensacola, USA.
Cureus. 2021 Aug 2;13(8):e16827. doi: 10.7759/cureus.16827. eCollection 2021 Aug.
Abnormal calcium/calcinosis/creatinine in Down syndrome (ABCD syndrome) is a very rare condition with no clear etiology. In this paper, we describe our clinical encounter with this disease. We report the case of an 11-month-old male infant with Down syndrome (DS) who presented to the hospital with intractable vomiting and decreased oral intake and urine output. The evaluation revealed an acute kidney injury (AKI) and hypercalcemia. Although his AKI improved with intravenous hydration, his hypercalcemia persisted. Extensive studies were notable for an elevated urinary excretion of calcium and bilateral medullary nephrocalcinosis seen on renal ultrasound (US). As a result, he was diagnosed with ABCD syndrome. Dietary calcium restriction was implemented. During his follow-up visit with a pediatric endocrinologist, his serum calcium was found to be normalized. To our knowledge, this is only the seventh case report on ABCD syndrome in the literature.
唐氏综合征中的异常钙/钙质沉着/肌酐(ABCD综合征)是一种非常罕见的病症,病因尚不明确。在本文中,我们描述了我们对该疾病的临床诊治过程。我们报告了一例11个月大的唐氏综合征男婴病例,该患儿因顽固性呕吐、经口摄入量和尿量减少入院。评估显示存在急性肾损伤(AKI)和高钙血症。尽管通过静脉补液他的急性肾损伤有所改善,但高钙血症仍持续存在。大量检查显示尿钙排泄增加,肾脏超声(US)检查发现双侧髓质肾钙质沉着。因此,他被诊断为ABCD综合征。实施了饮食钙限制。在他随访儿科内分泌科医生期间,发现他的血清钙已恢复正常。据我们所知,这是文献中关于ABCD综合征的第七例病例报告。