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编码磷脂酶A1的DDHD1基因突变是导致视网膜病变和伴有脑铁沉积的神经退行性变的新原因。

Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation.

作者信息

Dard Rodolphe, Meyniel Claire, Touitou Valérie, Stevanin Giovanni, Lamari Foudil, Durr Alexandra, Ewenczyk Claire, Mochel Fanny

机构信息

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.

出版信息

Eur J Med Genet. 2017 Dec;60(12):639-642. doi: 10.1016/j.ejmg.2017.08.015. Epub 2017 Aug 14.

DOI:10.1016/j.ejmg.2017.08.015
PMID:28818478
Abstract

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.

摘要

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。

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