cystic kidney - traducción al árabe
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cystic kidney - traducción al árabe

CONGENITAL OR ACQUIRED KIDNEY DISORDER CHARACTERIZED BY THE PRESENCE OF RENAL CYSTS
Cystic kidney diseases; Kidney diseases, cystic

cystic kidney      
‎ كُلْيَةٌ كيسِيَّة‎
renal cyst         
ABNORMAL FLUID FILLED SAC WITHIN THE KIDNEY, EITHER ACQUIRED OR CONGENITAL
Renal Cyst; Kidney cyst; Bosniak score; Bosniak classification; Bosniak class; Bosniak scale
‎ كيسَةٌ كُلْوِيَّة‎
medullary cystic disease         
  • Kidney biopsy/micrograph
  • Proximal convoluted tubule
  • Chromosome 16
  •  1. Glomerulus, 2. Efferent arteriole, 3. Bowman's capsule, 4. Proximal convoluted tubule, 5. Cortical collecting duct, 6. Distal convoluted tubule, 7. Loop of Henle, 8. Papillary duct, 9. Peritubular capillaries, 10. Arcuate vein, 11. Arcuate artery, 12. Afferent arteriole, 13. Juxtaglomerular apparatus.
INHERITED FORM OF CYSTIC KIDNEY DISEASE LEADING TO FIBROSIS AND IMPAIRED RENAL FUNCTION THAT IS CAUSED BY MUTATIONS IN THE UMOD GENE, WHICH ENCODES UROMODULIN/TAMM-HORSFALL MUCOPROTEIN
Medullary cystic disease; Medullary cystic renal disease; Autosomal-dominant medullary cystic kidney disease
الدَّاءُ الكِيسِيُّ اللُّبِّيّ

Definición

cystic fibrosis
Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult.
N-UNCOUNT

Wikipedia

Cystic kidney disease

Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life. Cystic disease may involve one or both kidneys and may, or may not, occur in the presence of other anomalies. A higher incidence is found in males and prevalence increases with age. Renal cysts have been reported in more than 50% of patients over the age of 50. Typically, cysts grow up to 2.88 mm annually and may cause related pain and/or hemorrhage.

Of the cystic kidney diseases, the most common is polycystic kidney disease with two sub-types: the less prevalent autosomal recessive and more prevalent autosomal dominant. Autosomal recessive polycystic kidney disease (ARPKD) is primarily diagnosed in infants and young children while autosomal dominant polycystic kidney disease (ADPKD) is most often diagnosed in adulthood.

Another example of cystic kidney disease is Medullary sponge kidney.