Oligomeganephronia (Q46440): Difference between revisions

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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.
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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.
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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.

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