Oligomeganephronia (Q46440): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Hipoplasia renal oligomeganefrônica é um defeito grave de desenvolvimento de ambos os rins, caracterizado por um número reduzido de néfrons (a unidade funcional do rim), glomérulos hipertróficos com diâmetros duas vezes maiores do que o normal, túbulos hipertróficos e espessamento da cápsula de Bowman, ocorrendo na ausência de uma malformação do trato urinário. | |||
| description / en | description / en | ||
Oligomeganephronic renal hypoplasia is a severe developmental defect of both kidneys characterised by a reduced number of nephrons (the functional unit of the kidney), hypertrophic glomeruli with diameters twice the normal size, hypertrophic tubules and thickening of Bowman's capsule, occurring in the absence of a urinary tract malformation. | |||
Revision as of 15:01, 13 August 2026
Oligomeganephronic renal hypoplasia is a severe developmental defect of both kidneys characterised by a reduced number of nephrons (the functional unit of the kidney), hypertrophic glomeruli with diameters twice the normal size, hypertrophic tubules and thickening of Bowman's capsule, occurring in the absence of a urinary tract malformation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB30.4 |
||
| English | Oligomeganephronia |
Oligomeganephronic renal hypoplasia is a severe developmental defect of both kidneys characterised by a reduced number of nephrons (the functional unit of the kidney), hypertrophic glomeruli with diameters twice the normal size, hypertrophic tubules and thickening of Bowman's capsule, occurring in the absence of a urinary tract malformation. |
