M. Ciccarese et al., Identification of a new mutation in the alpha 4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia, NEPH DIAL T, 16(10), 2001, pp. 2008-2012
Background. Alport syndrome (AS) is a hereditary disease of the glomerular
basement membrane in the kidney characterized by progressive renal failure,
sensorineural deafness. and/or ocular abnormalities. In contrast to the we
ll-known X-linked phenotype, very little is known about the autosomal domin
ant form. Rare autosomal forms of AS have been described with mutations in
COL4A3 and COL4A4 at chromosome region 2q35-q37, but there have been no des
criptions of dominant forms due to a mutation in COL4A4.
Methods. We describe a Sardinian family with a classical AS-phenotype plus
hypercholesterolaemia, a clinical feature also present in Fechtner syndrome
(FS), a disease that segregates as an autosomal dominant trait.
Results. A suggestive linkage (LOD= 2.7) between AS and the COL4A3/A4 locus
at 2q35-q37 was identified. Other candidate collagen genes encoding baseme
nt membrane collagen (COL4A1/A2 and COL4A5/A6) were excluded by linkage ana
lysis (13q33-q34 and Xq22), or by sequence (COL4A3). DNA sequence analysis
of the COL4A4 gene revealed that the Lys325Asn mutation was present in all
affected family members, but was absent in all unaffected members and in a
random sample of the Sardinian population. A clear indication of a gene-dos
age effect was seen in the most severely affected family member, since she
carried the mutation in the homozygous form.
Conclusions. These data confirm the importance of collagen 4A4 as a compone
nt in the structural integrity of the glomerular basement membrane and conf
irm the phenotypic and genetic heterogeneity of collagen disorders.