ReviewHippokratia2013
X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure.
Review in Hippokratia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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Who cites it
24 citing papers in PubMed, 42 citations in OpenAlex.
- Phenotype-genotype correlations in patients with Alport syndrome from the Polish population.Journal of nephrology · 2025Article
- Article
- Identification of novel COL4A5 variants and prenatal diagnosis in three large families.Scientific reports · 2025Article
- A variant of unknown significance in the COL4A5 gene-related renal disease: A novel case report.SAGE open medical case reports · 2024Article
- Review
- Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea.Scientific reports · 2023Article
- Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study.European journal of human genetics : EJHG · 2022Article
- Article
- Genotype-Phenotype Correlations for PathogenicFrontiers in medicine · 2022Review
- Guidelines for Genetic Testing and Management of Alport Syndrome.Clinical journal of the American Society of Nephrology : CJASN · 2022Article
- An overlap of Alport syndrome and rheumatoid arthritis in a patient and literature review.BMC nephrology · 2019Review
- Genotype-phenotype correlation and prognostic impact in Chinese patients with Alport Syndrome.Molecular genetics & genomic medicine · 2019Article
- Article
- A Nonsense Mutation in COL4A4 Gene Causing Isolated Hematuria in Either Heterozygous or Homozygous State.Frontiers in genetics · 2019Article
- The Hypomorphic Variant p.(Gly624Asp) inFrontiers in pediatrics · 2019Article
- Acute kidney injury due to thin basement membrane disease mimicking Deferasirox nephrotoxicity: a case report.BMC nephrology · 2018Article
- Identification of a NovelFrontiers in genetics · 2018Article
- RNA-seq of serial kidney biopsies obtained during progression of chronic kidney disease from dogs with X-linked hereditary nephropathy.Scientific reports · 2017Article
- Functional assessment of a novel COL4A5 splice region variant and immunostaining of plucked hair follicles as an alternative method of diagnosis in X-linked Alport syndrome.Pediatric nephrology (Berlin, Germany) · 2017Article
- Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.Pediatric nephrology (Berlin, Germany) · 2016Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Alport syndrome (ATS) results from X-linked, COL4A5 mutations (85%) or from autosomal recessive homozygous or compound heterozygous COL4A3/A4 mutations (15%), associated with alternate thinning and thickening as well as splitting and lamellation of the glomerular basement membranes. In contrast, familial microhematuria with thin basement membranes is thought to result from heterozygous COL4A3/A4 mutations. This absolute separation may not always be true. Renal biopsies and molecular genetics were used to study microhematuric families in the Hellenic population we serve. The COL4A5 gene was studied by PCR and direct re-sequencing for new mutations, while PCR-RFLP was used to identify more carriers of known COL4A5 and COL4A3/A4 mutations. Molecular genetics in two undiagnosed microhematuric Cypriot families, revealed COL4A5 mutation P628L indicating X-linked ATS. Of nine males, seven developed end stage kidney disease (ESKD) between 31 and 56, while two are well at 51 and 57, exhibiting microhematuria and thin basement membrane nephropathy (TBMN). COL4A5 mutation G624D was also identified in six Greek families. Seventy five members had DNA tests and 37 proved positive. Four positive males developed ESKD at 61, 51, 50 and 39 years, while the remaining and all females showed only microhematuria. A literature search revealed eight papers with six similar hypomorphic COL4A5 mutations presenting as phenocopies of TBMN. In conclusion, X-linked COL4A5 ATS mutations produce a phenotypic spectrum with a) classical ATS with early onset ESKD, neurosensory deafness and ocular defects b) males with only ESKD and late deafness and c) males due to missense mutations, such as G624D and P628L that may only exhibit microhematuria, TBMN, mild chronic renal failure (CRF) or late onset ESKD. Consequently when investigating "benign familial hematuria" these and other similar X-linked COL4A5 mutations should also be searched for.
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24470729PMC3872455W2147730695What OpenQuestion holds
Registered trials
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