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血浆植烷酸正常的变异型肢根型点状软骨发育不良(RCDP):一种亚型的临床生化特征及互补研究

Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studies.

作者信息

Barth P G, Wanders R J, Schutgens R B, Staalman C R

机构信息

Department of Pediatrics, University Hospital Amsterdam, Netherlands.

出版信息

Am J Med Genet. 1996 Mar 15;62(2):164-8. doi: 10.1002/(SICI)1096-8628(19960315)62:2<164::AID-AJMG9>3.0.CO;2-W.

Abstract

Rhizomelic chondrodysplasia calcificans punctata (RCDP) is an autosomal recessive peroxisomal disorder which affects phytanic acid oxidation and de novo biosynthesis of plasmalogens in liver and fibroblasts. Peroxisomal thiolase is present in its unprocessed precursor form (44 kDa). We studied a mentally retarded 9-year-old girl with cataracts and atypical bone dysplasia. Neurological findings were mild compared to classic RCDP. Plasma phytanic acid was normal. Results of de novo plasmalogen synthesis and phytanic acid oxidation studied in cultured skin fibroblasts were intermediate between normal controls and classic RCDP. Peroxisomal thiolase was present only as the unprocessed 44 kDa protein. Taken together these results suggest that we are dealing with a variant form of RCDP with clinical and biochemical abnormalities much milder as compared to classic RCDP. In order to establish the genetic relationship between our patient and classic RCDP patients complementation studies were carried out. Earlier studies had already shown that fibroblasts from all RCDP patients studied belong to a single complementation group. Fibroblasts from our patient could also be assigned to this complementation group suggesting that the phenotypic variability results from different mutations within the same gene.

摘要

点状钙化性肢根型软骨发育不良(RCDP)是一种常染色体隐性过氧化物酶体疾病,它会影响植烷酸氧化以及肝脏和成纤维细胞中缩醛磷脂的从头生物合成。过氧化物酶体硫解酶以未加工的前体形式(44 kDa)存在。我们研究了一名患有白内障和非典型骨骼发育异常的9岁智力发育迟缓女孩。与典型的RCDP相比,其神经学表现较轻。血浆植烷酸水平正常。在培养的皮肤成纤维细胞中进行的从头缩醛磷脂合成和植烷酸氧化研究结果介于正常对照和典型RCDP之间。过氧化物酶体硫解酶仅以未加工的44 kDa蛋白形式存在。综合这些结果表明,我们正在研究的是一种RCDP的变异形式,与典型RCDP相比,其临床和生化异常要轻得多。为了确定我们的患者与典型RCDP患者之间的遗传关系,进行了互补研究。早期研究已经表明,所有研究的RCDP患者的成纤维细胞都属于单一互补组。我们患者的成纤维细胞也可归为该互补组,这表明表型变异性是由同一基因内的不同突变引起的。

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