由于PTH基因突变导致婴儿期持续性低血症的罕见原因
Savita Khadse1, Vrushali Satish Takalikar1, Radha Ghildiyal1
1Pediatrics, Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, Maharashtra, India.
BMJ case reports
|September 12, 2023
概括
新生儿持续的低血症可能表明内分泌问题. 这一病例突出显示了一种罕见的先天性隔离性甲状腺功能低下症,由同卵性甲状腺上腺激素 (PTH) 基因突变引起.
科学领域:
- 儿科内分泌学 儿科内分泌学
- 遗传学 遗传学 是一个
- 新生儿医学 新生儿医学
背景情况:
- 低血症在新生儿中很常见,通常是短暂的.
- 持续的低血可能暗示内分泌系统疾病,包括低甲状腺症.
- 遗传因素,如迪乔治综合征或特定基因突变 (GCM2,CaSR,PTH) 是已知的原因.
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