Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Study of the True Clinical Progression of Autosomal Dominant Alport Syndrome in a European Population.

Kidney & blood pressure research - 1 Jan 2015

Rosado Consolación, Bueno Elena, Felipe Carmen, Valverde Sebastián, González-Sarmiento Rogelio

Abstract excerpt

BACKGROUND/AIMS: Autosomal dominant Alport syndrome represents 5% of all Alport syndrome cases. This entity presents a different clinical expression from the recessive inheritance pattern and the X chromosome-linked pattern, because it is mild and it shows a late onset, which in many cases even goes unnoticed. METHODS: We carried out a descriptive observational and retrospective clinical study on 19 patients from...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autoantigens
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Collagen Type IV

Share to Europe

Share to Family

Share to Hearing

Share to Nephritis, Hereditary

Source

Identifiers

PMID: 26277931
DOI: 10.1159/000368519

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Study of the True Clinical Progression of Autosomal Dominant Alport Syndrome in a European Population.PMID 26277931Read ↗

Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.Semantic proximity Read ↗

Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.Semantic proximity Read ↗

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.Semantic proximity Read ↗

Alport Syndrome in Women and Girls.Semantic proximity Read ↗

[From Alport syndrome to benign familial hematuria: clinical and genetic aspect].Semantic proximity Read ↗

A review of clinical characteristics and genetic backgrounds in Alport syndrome.Semantic proximity Read ↗

Renal, auricular, and ocular outcomes of Alport syndrome and their current management.Semantic proximity Read ↗

Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects.Semantic proximity Read ↗

Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome.Semantic proximity Read ↗

Autosomal dominant Alport's syndrome: study of a large Tunisian family.Semantic proximity Read ↗

Natural history of genetically proven autosomal recessive Alport syndromeSemantic proximity Read ↗

Alport syndrome in a Kazakh family: a case study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.