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肺动脉高压(pulmonary arterial hypertension,PAH)和肾血栓性微血管病(renal thrombotic microangiopathy,rTMA)是儿童非常罕见的疾病,分别可导致死亡和终末期肾脏疾病,尚未有两者同时发生的研究报道。该研究旨在对5个PAH伴rTMA患儿的临床、生化和遗传学方面的指标进行观察分析。
Pulmonary arterial hypertension (PAH) and renal thrombotic microangiopathy (rTMA) are very rare childhood diseases that cause death and end-stage renal disease, respectively. There have been no reports of both studies. The aim of this study was to investigate the clinical, biochemical and genetic parameters of 5 PAH patients with rTMA.