Autosomal dominant polycystic kidney disease associated with familial sensorineural deafness

被引:0
|
作者
Mora, C [1 ]
Navarro, JF [1 ]
García, J [1 ]
Gallego, E [1 ]
Macía, M [1 ]
Méndez, ML [1 ]
Chahin, J [1 ]
Rivero, A [1 ]
机构
[1] Hosp Ntra Sra Candelaria, Dept Nephrol, SC Tenerife 38010, Spain
来源
关键词
ADPKD; hereditary deafness; phenotypic variability;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by both renal and non-renal disorders. Extrarenal involvement includes noncystic manifestations such as cardiovascular abnormalities, colonic diverticula and intracranial aneurysms. Familial sensorineural hearing loss (SNHL) has been included in the definition of Alport's syndrome. However, other types of nephropathy have been occasionally associated with hereditary deafness. The association of ADPKD with hereditary SNHL has not been previously documented. We report a family with ADPKD associated with bilateral sensorineural dearness in a pedigree of four affected members in four generations.
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页码:63 / 65
页数:3
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