Stavrou C, Pierides A, Zouvani I, Kyriacou K, Antignac C, Neophytou P, Christodoulou K, Deltas C C
Department of Nephrology, Ministry of Health, Nicosia, Cyprus.
Am J Med Genet. 1998 May 1;77(2):149-54. doi: 10.1002/(sici)1096-8628(19980501)77:2<149::aid-ajmg8>3.0.co;2-n.
We describe a large Cypriot family with an interstitial type of nephropathy, inherited as an autosomal dominant trait that led to end stage renal failure between 51 to 78 years of age (mean 62.2 years). Twenty-three people are known to be affected, but several younger relatives with normal renal function may remain undiagnosed because of the absence of precise clinical and laboratory diagnostic criteria. This nephropathy is associated with medullary renal cysts, hypertension, hyperuricemia, and gout. Several relatives have typical medullary cystic disease (MCD), while in the others the findings are compatible with this diagnosis. Due to the similarity of clinical and pathologic findings, earlier reports had suggested that MCD may be allelic to autosomal recessive familial juvenile nephronophthisis, which was mapped recently to chromosome band 2q13. Linkage analysis of the present family with a closely linked marker excluded linkage to the above locus. Linkage was also excluded to the PKD1 locus of adult polycystic kidney disease type 1, and up to 5 cM on either side, on chromosome 16. We suggest that because of the element of hyperuricemia and gout found in this family, although with reduced penetrance, it may represent a variant of autosomal dominant MCD of the adult type. This variability may be the result of allelic or locus heterogeneity. Molecular genetic approaches including linkage analysis on appropriate families will certainly assist in classifying such related genetically heterogeneous disorders.
我们描述了一个塞浦路斯大家族,其患有间质性肾病,呈常染色体显性遗传,可导致51至78岁(平均62.2岁)出现终末期肾衰竭。已知有23人患病,但由于缺乏精确的临床和实验室诊断标准,一些肾功能正常的年轻亲属可能仍未被诊断出来。这种肾病与肾髓质囊肿、高血压、高尿酸血症和痛风有关。一些亲属患有典型的髓质囊性疾病(MCD),而其他亲属的检查结果也符合该诊断。由于临床和病理表现相似,早期报告曾认为MCD可能与常染色体隐性遗传性青少年肾单位肾痨等位,后者最近被定位到2q13染色体带。对该家族与一个紧密连锁标记进行连锁分析,排除了与上述位点的连锁关系。同时也排除了与成年型多囊肾病1型的PKD1位点以及16号染色体上其两侧各5厘摩区域的连锁关系。我们认为,鉴于该家族中存在高尿酸血症和痛风因素,尽管外显率降低,但它可能代表成年型常染色体显性MCD的一种变异型。这种变异性可能是等位基因或位点异质性的结果。包括对合适家族进行连锁分析在内的分子遗传学方法肯定有助于对这类相关的基因异质性疾病进行分类。