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患有施姆克免疫性骨发育不良的两兄弟的不同生长模式。

Different growth patterns in two siblings with Schimke immuno-osseous-dysplasia.

作者信息

Bokenkamp Arend, Bouts Antonia, van der Weerd Neeltje, Levtchenko Elena, Haffner Dieter, Zivicnjak Miroslav

机构信息

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.

出版信息

Pediatr Nephrol. 2025 Mar;40(3):701-703. doi: 10.1007/s00467-024-06503-5. Epub 2024 Sep 18.

DOI:10.1007/s00467-024-06503-5
PMID:39292251
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11753360/
Abstract

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).

摘要

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)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c102/11753360/f28559e8dd20/467_2024_6503_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c102/11753360/f28559e8dd20/467_2024_6503_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c102/11753360/f28559e8dd20/467_2024_6503_Fig1_HTML.jpg

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本文引用的文献

1
Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells.Schimke 免疫骨发育不良表型扩展:肾脏和泌尿道先天异常及 NK 细胞改变。
Int J Mol Sci. 2020 Nov 15;21(22):8604. doi: 10.3390/ijms21228604.
2
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia.施姆克免疫性骨发育不良中肾脏表型变异性低但肾外表型变异性高。
PLoS One. 2017 Aug 10;12(8):e0180926. doi: 10.1371/journal.pone.0180926. eCollection 2017.
3
Schimke versus non-Schimke chronic kidney disease: an anthropometric approach.
施姆克型与非施姆克型慢性肾脏病:一种人体测量学方法
Pediatrics. 2006 Aug;118(2):e400-7. doi: 10.1542/peds.2005-2614. Epub 2006 Jun 30.
4
R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia.与轻度施姆克免疫性骨发育不良相关的SMARCAL1基因R561C错义突变。
Pediatr Nephrol. 2005 Dec;20(12):1724-8. doi: 10.1007/s00467-005-2047-x. Epub 2005 Oct 20.
5
Schimke-immuno-osseous dysplasia: new mutation with weak genotype-phenotype correlation in siblings.施姆克免疫性骨发育不良:同胞中具有弱基因型-表型相关性的新突变。
Am J Med Genet A. 2005 Jun 1;135(2):202-5. doi: 10.1002/ajmg.a.30691.