骨表型总是存在的,但在PAPSS2缺乏症中,雄激素过量较少见

Didem Helvacıoğlu1, Tülay Güran1

  • 1Marmara University Faculty of Medicine, Department of Pediatric Endocrinology and Diabetes, İstanbul, Turkey

概括

3-adenosine 5-硫酸合成酶2 (PAPSS2) 缺乏症是一种罕见的遗传性疾病. 本综述总结了79名报告患者的临床,分子和生化特征,重点关注骨发育不良和雄激素过量.

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