CPOX,

Elif Kelestemur1, Murat Hakki Yarar2, Busra Gurpinar Tosun1

  • 1Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Başıbüyük, Istanbul 34854, Turkey.

概括

由CPOX基因突变引起的硬性皮质症可以通过影响线粒体类固醇酶导致原发性上腺功能不足 (PAI). 这项研究描述了患有硬骨症的兄弟姐妹的PAI,揭示了重叠的临床症状.

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