cystic medial necrosis - traduction vers arabe
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  1. Dictionnaires
  2. Dictionnaire anglais-arabe
  3. cystic medial necrosis

cystic medial necrosis - traduction vers arabe

MEDICAL CONDITION
Cystic medial necrosis; Cystic medial degeneration

cystic medial necrosis         
‎ النَّخَرُ الكِيْسِيُّ للغِلالَةِ الوَسْطانِيَّة‎
fibrocystic disease of the pancreas         
  • 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
‎ الداءُ الكيسِيُّ اللِّيفِيُّ في البنكرياس‎
mucoviscidosis         
  • 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
‎ تَلَزُّجُ المُخَاطِ,تَلَيُّفُ البَنْكِرياسِ الكيسِيّ‎

Définition

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

Familial thoracic aortic aneurysm

Familial thoracic aortic aneurysm is an autosomal dominant disorder of large arteries.

There is an association between familial thoracic aortic aneurysm and Marfan syndrome as well as other hereditary connective tissue disorders.

https://en.wikipedia.org/wiki/Familial thoracic aortic aneurysm
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