Ventricular septal defect in a child with Alport syndrome: a case report

被引:0
作者
Pier Paolo Bassareo
Andrea Raffaele Marras
Giuseppe Mercuro
机构
[1] University of Cagliari,Department of Cardiovascular and Neurological Sciences
[2] University of Cagliari,Study Center for Cardiac Disease in Pediatric Age
来源
BMC Cardiovascular Disorders | / 10卷
关键词
Congenital Heart Disease; Clonidine; Ventricular Septal Defect; Ventricular Septal Defect; Glomerular Basal Membrane;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 87 条
[1]  
Alport AC(1927)Hereditary familial congenital haemorrhagic nephritis BMJ i 504-506
[2]  
Williamson DAJ(1961)Alport's syndrome of hereditary nephritis with deafness Lancet ii 1321-1323
[3]  
Heidet L(2009)The renal lesions of Alport syndrome J Am Soc Nephrol 20 1210-1215
[4]  
Gubler MC(1992)Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome Kidney Int 42 115-126
[5]  
Kashtan CE(1997)Alport's syndrome J Med Genet 34 326-330
[6]  
Kim Y(2003)X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study J Am Soc Nephrol 14 2603-2610
[7]  
Flinter F(1990)Alport's syndrome: genetic evaluation of personal data concerning twelve families Contrib Nephrol 80 126-130
[8]  
Jais JP(1993)Hereditary nephritis (Alport's syndrome) - clinical profile and inheritance in 28 kindreds Nephrol Dial Transplant 8 690-695
[9]  
Knebelmann B(1997)Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure Kidney Int 51 1596-1601
[10]  
Giatras I(1996)A mutation causing Alport syndrome with tardive hearing loss is common in the Western United States Am J Hum Genet 58 1157-1165