Service de génétique, CLAD Ouest, CHU Rennes, Rennes, France.
Service de génétique, CLAD Ouest, CHU Rennes, Rennes, France; CNRS UMR6290 Institut de génétique et développement de Rennes IGDR, Université de Rennes, Rennes, France.
Eur J Med Genet. 2020 Dec;63(12):104087. doi: 10.1016/j.ejmg.2020.104087. Epub 2020 Oct 31.
ATP7A-related copper transport disorders are classically separated in three pathologies according to their severity, all inherited in an X-linked recessive manner: Menkes disease (MD, OMIM #309400) which represent more than 90% of cases; occipital Horn Syndrome (OHS, OMIM #304150) and ATP7A-related distal motor neuropathy also named X-linked distal spinal muscular atrophy-3 (SMAX3, OMIM #300489) (Kennerson et al., 2010). Although there is no clear cut correlation between Cu and ceruloplasmin levels in ATP7A related disorders, these three entities probably represent a continuum partly depending on residual functional ATP7A protein (Møller, 2015). Thus far OHS and SMAX3 only partially overlap. In fact patients with OHS usually have no distal motor neuropathy signs but, on the other hand, occipital horns, which are the main sign of OHS, have not been described in SMAX3 patient. We describe here a patient bearing a missense ATP7A mutation with associated signs of distal motor neuropathy as well as occipital horns, confirming that OHS and SMAX3 are a continuum.
ATP7A 相关的铜转运障碍根据其严重程度经典地分为三种病理学,均以 X 连锁隐性方式遗传:Menkes 病(MD,OMIM#309400),占 90%以上的病例;枕骨角综合征(OHS,OMIM#304150)和 ATP7A 相关的远端运动神经病也称为 X 连锁远端脊肌萎缩症-3(SMAX3,OMIM#300489)(Kennerson 等人,2010 年)。尽管在 ATP7A 相关疾病中铜和铜蓝蛋白水平之间没有明显的相关性,但这三种疾病可能代表一种连续体,部分取决于残余功能的 ATP7A 蛋白(Møller,2015 年)。到目前为止,OHS 和 SMAX3 仅部分重叠。事实上,OHS 患者通常没有远端运动神经病的迹象,但另一方面,OHS 的主要特征——枕骨角,在 SMAX3 患者中尚未描述。我们在这里描述了一名携带错义 ATP7A 突变的患者,其伴有远端运动神经病和枕骨角的迹象,证实了 OHS 和 SMAX3 是一个连续体。