Ilan T, Shohat T, Tobar A, Magal N, Yahav M, Halpern G J, Rechavi G, Shohat M
Department of Pediatric Hematology and Oncology, Sheba Medical Center, Tel-Hashomer, Israel.
Isr Med Assoc J. 2001 Jul;3(7):488-91.
Familial nephritis is a heterogeneous group of disorders caused by several genetic conditions such as Alport syndrome, glomerulonephritic syndromes, and unclassified nephritis without deafness or ocular defects.
To describe a family of Iraqi Jewish origin, several of whose members suffer from non-syndromic renal failure without deafness or ocular defects and where transmission is by autosomal dominant inheritance. We present the case histories of four family members and describe the molecular analysis performed in order to seek a possible linkage to one of the genes causing Alport or Alport-like syndromes.
We investigated all family members over the age of 18 for evidence of renal failure. We also extracted DNA and carried out molecular linkage analysis with polymorphic markers in each of the known loci involved in Alport and Alport-like syndromes.
Histology of the renal biopsy specimens showed non-specific findings. Linkage was excluded for all the Alport and Alport-like syndrome loci.
The condition suffered by several members of this family seems to represent a unique autosomal dominant type of progressive hereditary nephritis, characterized by hypertension and progressive renal failure without significant hematuria or proteinuria. The main histological changes are non-specific in the early stage of the disease. Our study rules out all the currently known genes that cause Alport syndrome as being responsible for the basic defect in this type of nephritis.
家族性肾炎是一组由多种遗传疾病引起的异质性疾病,如阿尔波特综合征、肾小球肾炎综合征以及无耳聋或眼部缺陷的未分类肾炎。
描述一个伊拉克犹太裔家族,其多名成员患有无耳聋或眼部缺陷的非综合征性肾衰竭,且呈常染色体显性遗传。我们展示了四名家族成员的病例史,并描述了为寻找与导致阿尔波特或类阿尔波特综合征的基因之一可能存在的连锁关系而进行的分子分析。
我们对所有18岁以上的家族成员进行了肾衰竭证据调查。我们还提取了DNA,并对参与阿尔波特和类阿尔波特综合征的每个已知基因座中的多态性标记进行了分子连锁分析。
肾活检标本的组织学检查显示非特异性结果。所有阿尔波特和类阿尔波特综合征基因座的连锁关系均被排除。
该家族几名成员所患疾病似乎代表一种独特的常染色体显性进行性遗传性肾炎,其特征为高血压和进行性肾衰竭,无明显血尿或蛋白尿。疾病早期的主要组织学变化是非特异性的。我们的研究排除了所有目前已知的导致阿尔波特综合征的基因是这种类型肾炎基本缺陷病因的可能性。