cystic disease of lung - перевод на арабский
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cystic disease of lung - перевод на арабский

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
  • 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.

cystic disease of lung      
‎ داءُ الرِّئَةِ الكيسِيّ‎
medullary cystic disease         
الدَّاءُ الكِيسِيُّ اللُّبِّيّ
medullary cystic disease         
‎ الدَّاءُ الكِيسِيُّ اللُّبِّيّ,السُّلُّ الكُلْوِيُّ اليَفَعِيُّ العائِلِيّ, الدَّاءُ اللُّبِّيُّ الكِيْسِيّ‎

Определение

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

Википедия

Medullary cystic kidney disease

Medullary cystic kidney disease (MCKD) is an autosomal dominant kidney disorder characterized by tubulointerstitial sclerosis leading to end-stage renal disease. Because the presence of cysts is neither an early nor a typical diagnostic feature of the disease, and because at least 4 different gene mutations may give rise to the condition, the name autosomal dominant tubulointerstitial kidney disease (ADTKD) has been proposed, to be appended with the underlying genetic variant for a particular individual. Importantly, if cysts are found in the medullary collecting ducts they can result in a shrunken kidney, unlike that of polycystic kidney disease. There are two known forms of medullary cystic kidney disease, mucin-1 kidney disease 1 (MKD1) and mucin-2 kidney disease/uromodulin kidney disease (MKD2). A third form of the disease occurs due to mutations in the gene encoding renin (ADTKD-REN), and has formerly been known as familial juvenile hyperuricemic nephropathy type 2.