Ghazawi Feras M, Proulx Etienne Saint-Cyr, Jafarian Fatemeh
Division of Dermatology, University of Ottawa, Ottawa, ON, Canada.
Hôpital de la Cité-de-la-Santé, Laval, QC, Canada.
SAGE Open Med Case Rep. 2019 May 19;7:2050313X19850359. doi: 10.1177/2050313X19850359. eCollection 2019.
Lipoid proteinosis is a rare autosomal recessive genodermatosis that is caused by loss-of-function mutations in the extracellular matrix protein 1 gene. This study identifies a novel nonsense mutation in exon 9 of the extracellular matrix protein 1 gene associated with lipoid proteinosis, contributing to recent advances in our understanding of the molecular genetics underlying this disease. It is important to identify the mutations in the extracellular matrix protein 1 gene that are associated with lipoid proteinosis and how these affect protein function. Understanding the molecular basis for such genetic disorders may lead to novel therapeutic approaches for treating hereditary genodermatoses.
类脂蛋白沉积症是一种罕见的常染色体隐性遗传性皮肤病,由细胞外基质蛋白1基因的功能丧失性突变引起。本研究在与类脂蛋白沉积症相关的细胞外基质蛋白1基因第9外显子中鉴定出一种新的无义突变,有助于我们对该疾病潜在分子遗传学的最新认识。识别与类脂蛋白沉积症相关的细胞外基质蛋白1基因突变以及这些突变如何影响蛋白质功能非常重要。了解此类遗传疾病的分子基础可能会带来治疗遗传性皮肤病的新方法。