| Literature DB >> 28818478 |
Rodolphe Dard1, Claire Meyniel2, Valérie Touitou3, Giovanni Stevanin4, Foudil Lamari5, Alexandra Durr6, Claire Ewenczyk6, Fanny Mochel7.
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.Entities:
Keywords: DDHD1; Hereditary spastic paraplegia; NBIA; Phospholipids; Retinopathy
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Year: 2017 PMID: 28818478 DOI: 10.1016/j.ejmg.2017.08.015
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708