cystic kidney - définition. Qu'est-ce que cystic kidney
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Qu'est-ce (qui) est cystic kidney - définition


Cystic kidney disease         
CONGENITAL OR ACQUIRED KIDNEY DISORDER CHARACTERIZED BY THE PRESENCE OF RENAL CYSTS
Cystic kidney diseases; Kidney diseases, cystic
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.
Renal cyst         
  • A Bosniak category IIF cyst. This one is 3 cm wide, with calcifications within its wall, seen as very radiodense (white in this presentation) areas in its margins. There is also a septation which is calcified. Yet, the cyst does not show enhancement (uptake of contrast).
  • pelvises]]. The fluid accumulations are thus peripelvic cysts.
  • website=Pathology Outlines}} Topic Completed: 1 November 2011. Minor changes: 1 October 2019</ref> but this case has a somewhat thicker fibrous layer. H&E stain.
  • alt=Simple renal cyst.jpg
ABNORMAL FLUID FILLED SAC WITHIN THE KIDNEY, EITHER ACQUIRED OR CONGENITAL
Renal Cyst; Kidney cyst; Bosniak score; Bosniak classification; Bosniak class; Bosniak scale
A renal cyst is a fluid collection in or on the kidney. There are several types based on the Bosniak classification.
cystic fibrosis         
  • Health problems associated with cystic fibrosis
  • The CFTR protein is a channel protein that controls the flow of H<sub>2</sub>O and Cl<sup>−</sup> ions in and out of cells inside the lungs. When the CFTR protein is working correctly, ions freely flow in and out of the cells. However, when the CFTR protein is malfunctioning, these ions cannot flow out of the cell due to a blocked channel. This causes cystic fibrosis, characterized by the buildup of thick mucus in the lungs.
  • The location of the ''CFTR'' gene on chromosome 7
  • Respiratory infections in CF vary according to age.<br><br>Green = ''[[Pseudomonas aeruginosa]]''<br>Brown = ''[[Staphylococcus aureus]]''<br>Blue = ''[[Haemophilus influenzae]]''<br>Red = ''[[Burkholderia cepacia]]'' complex
  • [[Dorothy Hansine Andersen]] first described cystic fibrosis in 1938.
  • script]])
  • Intracytoplasmic sperm injection can be used to provide fertility for men with cystic fibrosis.
AUTOSOMAL RECESSIVE DISEASE CHARACTERIZED BY THE BUILDUP OF MUCUS
Mucoviscidosis; Cistic fibrosis; Cystic Fiborsis; Cystic fibrosis allele; Cystic fibrose; Mucoviscidose; Viscoidosis; Mucuviscoidosis; Mucoviscoidosis; Mucoviscidopsis; Fibrocystic disease of the pancreas; Cystic Fibrosis; Cyctic fibrosis; Cystic Fibrosis (CF); History of Cystic fibrosis; Gene therapy for cystic fibrosis; Treatment of cystic fibrosis
Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult.
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