Human Molecular Genetics, Vol 7, 905-911, Copyright © 1998 by Oxford University Press
K Christodoulou, M Tsingis, C Stavrou, A Eleftheriou, P Papapavlou, PC Patsalis, P Ioannou, A Pierides and C Constantinou Deltas
There is a group of inherited cystic nephropathies that are characterized
by juvenile onset recessive inheritance (familial juvenile
nephronophthisis, FJN) or by adult onset dominant inheritance (medullary
cystic disease, MCD) and share similar clinico-pathological presentation to
the extent that they are usually grouped together under the term FJN/MCD
complex. The main symptoms consist of renal cyst formation in the medulla
or the corticomedullary junction and salt wasting. Although earlier reports
had suggested that one single gene may be responsible for this pathology,
recent reports have shown that the FJN complex itself comprises a
genetically heterogeneous group. Here we are presenting two large Cypriot
families that segregate autosomal dominant medullary cystic kidney disease
(ADMCKD) with hyperuricemia and gout and with very late age of onset (mean
62.2 and 51.5 years). We performed DNA linkage mapping using highly
polymorphic microsatellite markers and found linkage to marker locus
D1S1595 at 1q21 with a two-point lod score of 6.45 at Theta = 0.00.
Analysis of haplotypes and of critical recombinants enabled confinement of
the disease locus within an approximately 8 cM region between marker loci
D1S498 and D1S2125. FISH mapping with a large P1 clone confirmed the
physical localization within 1q21. The two families share the same disease
haplotype, thus suggesting their relationship through a common ancestor and
the possible existence of a single ADMCKD-causing mutation within these
families. To our knowledge this is the first genetic locus identified to
cause FJN/MCD pathology of the dominant adult type.
ARTICLES
Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease
Department of Molecular Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
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