Dard Rodolphe, Meyniel Claire, Touitou Valérie, Stevanin Giovanni, Lamari Foudil, Durr Alexandra, Ewenczyk Claire, Mochel Fanny
AP-HP, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, Paris, France; CHI Poissy St Germain-en-Laye, Département de Génétique, Cytogénétique et Biologie de la Reproduction, St Germain-en-Laye, France.
AP-HP, Département de Neurophysiologie, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Eur J Med Genet. 2017 Dec;60(12):639-642. doi: 10.1016/j.ejmg.2017.08.015. Epub 2017 Aug 14.
Defects of phospholipids remodelling and synthesis are inborn errors of metabolism responsible for various clinical presentations including spastic paraplegia, retinopathy, optic atrophy, myo- and cardiomyopathies, and osteo-cutaneous manifestations. DDHD1 encodes a phospholipase A1, which is involved in the remodelling of phospholipids. We previously described a relatively pure hereditary spastic paraplegia (HSP) phenotype associated with mutations in DDHD1. Here we report a complex form of HSP associated with retinal dystrophy and a pattern of neurodegeneration with brain iron accumulation (NBIA) on brain MRI, due to a novel homozygous mutation in DDHD1. This observation enlarges the clinical spectrum of DDHD1-associated disorders and sheds light on a new aetiology for syndromes associating retinopathy and NBIA. It also emphasizes the role of complex lipids in the retina.
磷脂重塑和合成缺陷是先天性代谢错误,可导致各种临床表现,包括痉挛性截瘫、视网膜病变、视神经萎缩、肌病和心肌病以及骨皮肤表现。DDHD1编码一种磷脂酶A1,参与磷脂的重塑。我们之前描述了一种与DDHD1突变相关的相对单纯的遗传性痉挛性截瘫(HSP)表型。在此,我们报告了一种复杂形式的HSP,伴有视网膜营养不良以及脑MRI上出现脑铁沉积(NBIA)的神经退行性变模式,这是由于DDHD1中一个新的纯合突变所致。这一观察结果扩大了DDHD1相关疾病的临床谱,并为视网膜病变和NBIA相关综合征的新病因提供了线索。它还强调了复合脂质在视网膜中的作用。