Sá Maria João Nabais, Rocha Júlio C, Almeida Manuela F, Carmona Carla, Martins Esmeralda, Miranda Vasco, Coutinho Miguel, Ferreira Rita, Pacheco Sara, Laranjeira Francisco, Ribeiro Isaura, Fortuna Ana Maria, Lacerda Lúcia
Department of Medical Genetics, Centro de Genética Médica Dr. Jacinto de Magalhães/Centro Hospitalar do Porto, Porto, Portugal.
Unit for Multidisciplinary Research in Biomedicine, Instituto de Ciências Biomédicas Abel Salazar/Universidade do Porto, Porto, Portugal.
JIMD Rep. 2016;26:53-60. doi: 10.1007/8904_2015_487. Epub 2015 Aug 25.
Infantile Refsum disease (IRD) is one of the less severe of Zellweger spectrum disorders (ZSDs), a group of peroxisomal biogenesis disorders resulting from a generalized peroxisomal function impairment. Increased plasma levels of very long chain fatty acids (VLCFA) and phytanic acid are biomarkers used in IRD diagnosis. Furthermore, an increased plasma level of phytanic acid is known to be associated with neurologic damage. Treatment of IRD is symptomatic and multidisciplinary.The authors report a 3-year-old child, born from consanguineous parents, who presented with developmental delay, retinitis pigmentosa, sensorineural deafness and craniofacial dysmorphisms. While the relative level of plasma C26:0 was slightly increased, other VLCFA were normal. Thus, a detailed characterization of the phenotype was essential to point to a ZSD. Repeatedly increased levels of plasma VLCFA, along with phytanic acid and pristanic acid, deficient dihydroxyacetone phosphate acyltransferase activity in fibroblasts and identification of the homozygous pathogenic mutation c.2528G>A (p.Gly843Asp) in the PEX1 gene, confirmed this diagnosis. Nutritional advice and follow-up was proposed aiming phytanic acid dietary intake reduction. During dietary treatment, plasma levels of phytanic acid decreased to normal, and the patient's development evaluation showed slow progressive acquisition of new competences.This case report highlights the relevance of considering a ZSD in any child with developmental delay who manifests hearing and visual impairment and of performing a systematic biochemical investigation, when plasma VLCFA are mildly increased. During dietary intervention, a biochemical improvement was observed, and the long-term clinical effect of this approach needs to be evaluated.
婴儿型雷夫叙姆病(IRD)是泽尔韦格谱系障碍(ZSD)中病情相对较轻的一种,ZSD是一组因过氧化物酶体功能普遍受损导致的过氧化物酶体生物发生障碍。血浆中极长链脂肪酸(VLCFA)和植烷酸水平升高是IRD诊断中使用的生物标志物。此外,已知血浆植烷酸水平升高与神经损伤有关。IRD的治疗是对症且多学科的。作者报告了一名3岁儿童,其父母为近亲结婚,该患儿出现发育迟缓、色素性视网膜炎、感音神经性耳聋和颅面部畸形。虽然血浆C26:0的相对水平略有升高,但其他VLCFA正常。因此,对表型进行详细特征描述对于明确ZSD至关重要。血浆VLCFA、植烷酸和降植烷酸水平反复升高,成纤维细胞中二羟基丙酮磷酸酰基转移酶活性缺乏,以及在PEX1基因中鉴定出纯合致病突变c.2528G>A(p.Gly843Asp),证实了这一诊断。建议给予营养建议并进行随访,目标是减少植烷酸的饮食摄入量。在饮食治疗期间,血浆植烷酸水平降至正常,对患者的发育评估显示其缓慢逐步获得新技能。本病例报告强调了对于任何有发育迟缓且伴有听力和视力损害的儿童考虑ZSD的相关性,以及当血浆VLCFA轻度升高时进行系统生化检查的重要性。在饮食干预期间,观察到生化指标有所改善,这种方法的长期临床效果有待评估。