Anjos Mariana M, Figueireido Ana M, Cardoso Patricia, Costa Filipa, Morais Julieta
Pediatrics, Centro Hospitalar do Médio Tejo, Torres Novas, PRT.
Cureus. 2024 Jan 30;16(1):e53233. doi: 10.7759/cureus.53233. eCollection 2024 Jan.
Seizures are the most common neurological disorder in pediatrics, and their initial approach aims at clinical stabilization. A thorough patient evaluation may provide important clues for the etiological diagnosis. A 12-month-old female child was observed in the emergency department after experiencing her first apyretic seizure. She had a history of congenital alopecia and, on physical examination, presented subtotal alopecia and milia. Initial investigation revealed hypocalcemia; therefore, intravenous calcium correction was started with a partial response. The analytical study was extended, revealing hypophosphatemia, elevated parathormone, and 1,25(OH) vitamin D with normal 25(OH) vitamin D. The genetic analysis confirmed hereditary vitamin D-resistant rickets (HVDRR). The integration of the findings was crucial to diagnostic reasoning and to guide further investigation. HVDRR is a rare disorder, with more severe clinical presentations associated with alopecia. Early diagnosis and treatment are fundamental to minimize the impact on growth and the development of other comorbidities.
癫痫发作是儿科最常见的神经系统疾病,其初始治疗旨在实现临床稳定。全面的患者评估可为病因诊断提供重要线索。一名12个月大的女童在经历首次无热惊厥后被送往急诊科。她有先天性脱发病史,体格检查发现部分脱发和粟丘疹。初步检查发现低钙血症;因此开始静脉补钙治疗,但仅有部分反应。进一步的分析研究发现低磷血症、甲状旁腺激素升高、1,25(OH)维生素D升高而25(OH)维生素D正常。基因分析确诊为遗传性维生素D抵抗性佝偻病(HVDRR)。综合各项检查结果对于诊断推理及指导进一步检查至关重要。HVDRR是一种罕见疾病,临床表现更为严重,常伴有脱发。早期诊断和治疗对于将其对生长及其他合并症发展的影响降至最低至关重要。