К содержанию
РецензированоEN2025

FEATURES OF THE COURSE OF ALPORT SYNDROME IN CHILDREN

Malika Mukaddasova (Student of the Fergana Medical Institute of Public Health. Scientific supervisor) · Iroda Alimova (Fergana, Uzbekistan.)

Теоретические аспекты становления педагогических наук · 175-176 · 2025

Аннотация

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.

Доказательный фрагмент

«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.»

Образец извлечения

Демо-превью

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. Полный текст публикации CiteX не хранит — доступ к первоисточнику открывается по DOI согласно лицензии издателя и выбранному плану.

DOI не указан
Цитирований
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Тип
Журнал
Страна
Узбекистан
Ключевые слова
Alport syndrome, collagen type IV, hereditary nephritis, hematuria, chronic renal failure, hearing loss, genetics.
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