FEATURES OF THE COURSE OF ALPORT SYNDROME IN CHILDREN

It has been established that in the last decade the incidence of Alport syndrome among children has increased, the disease has become more frequently diagnosed. Alport syndrome is a hereditary disease that affects the kidneys, hearing and vision organs. It is rare, but can lead to chronic renal failure and complete hearing loss in childhood. At the same time, timely diagnosis plays a major role in preventing early severe consequences.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-04-15
DOI
https://doi.org/10.5281/zenodo.15222618
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
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article

FEATURES OF THE COURSE OF ALPORT SYNDROME IN CHILDREN

Zenodo (CERN European Organization for Nuclear Research)
Gene expression and cancer classification
article

FEATURES OF THE COURSE OF ALPORT SYNDROME IN CHILDREN

article en

Abstract

It has been established that in the last decade the incidence of Alport syndrome among children has increased, the disease has become more frequently diagnosed. Alport syndrome is a hereditary disease that affects the kidneys, hearing and vision organs. It is rare, but can lead to chronic renal failure and complete hearing loss in childhood. At the same time, timely diagnosis plays a major role in preventing early severe consequences.

Zenodo (CERN European Organization for Nuclear Research)
Good health and well-being
Openalex Percentile: Top 56%
Gene expression and cancer classification
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FEATURES OF THE COURSE OF ALPORT SYNDROME IN CHILDREN · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS