Bokenkamp Arend, Bouts Antonia, van der Weerd Neeltje, Levtchenko Elena, Haffner Dieter, Zivicnjak Miroslav
Department of Pediatric Nephrology, Emma Children's Hospital, Meibergdreef 9, Amsterdam, NL-1105 AZ, The Netherlands.
Department of Nephrology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Pediatr Nephrol. 2025 Mar;40(3):701-703. doi: 10.1007/s00467-024-06503-5. Epub 2024 Sep 18.
Schimke immuno-osseous-dysplasia (SIOD) is an autosomal recessive systemic disease due to pathogenic variants in SMARCAL1. Manifestations include nephrotic syndrome (NS), kidney failure, T-cell dysfunction, vaso-occlusive disease, and disproportionate short stature, a general feature of this disease. Here, we present a markedly different growth pattern in two brothers with SIOD sharing the same homozygous R561C missense variant. The index patient presented at the age of 11 years with NS and severely disproportionate short stature, followed by kidney failure at the age of 16, and severely reduced adult height (z-score - 8.0). In contrast, the younger brother showed normal growth until the age of 8 years. Mild proteinuria was noted at the age of 4.5, followed by NS at 9.5 years, kidney failure at 11 years, progressive disproportionate stature, and reduced adult height (z-score - 4.5). Both brothers had comparable disproportion in adulthood (sitting height index z-score - 0.88 and - 1.44, respectively).
施姆克免疫性骨发育不良(SIOD)是一种常染色体隐性全身性疾病,由SMARCAL1基因的致病变异引起。其表现包括肾病综合征(NS)、肾衰竭、T细胞功能障碍、血管闭塞性疾病以及身材比例失调的矮小症,这是该疾病的一个普遍特征。在此,我们报告了两名患有SIOD且共享相同纯合R561C错义变异的兄弟明显不同的生长模式。索引患者11岁时出现NS和严重不成比例的矮小症,16岁时出现肾衰竭,成年身高严重降低(z评分-8.0)。相比之下,弟弟8岁前生长正常。4.5岁时出现轻度蛋白尿,9.5岁时出现NS,11岁时出现肾衰竭,逐渐出现身材比例失调以及成年身高降低(z评分-4.5)。两兄弟成年后身材比例失调程度相当(坐高指数z评分分别为-0.88和-1.44)。