cystic lymphangiectasis - traducción al árabe
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cystic lymphangiectasis - traducción al árabe

PATHOLOGIC DILATION OF LYMPH VESSELS
Lymphangiectasis

cystic lymphangiectasis      
‎ تَوَسُّعُ الأَوعِيَةِ اللِّمْفِيَّةِ الكيسِيّ,الوَرَمُ الوِعائِيُّ اللِّمْفِيُّ الكيسِيّ‎
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

Definición

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

Wikipedia

Lymphangiectasia

Lymphangiectasia, also known as "lymphangiectasis", is a pathologic dilation of lymph vessels. When it occurs in the intestines of dogs, and more rarely humans, it causes a disease known as "intestinal lymphangiectasia". This disease is characterized by lymphatic vessel dilation, chronic diarrhea and loss of proteins such as serum albumin and globulin. It is considered to be a chronic form of protein-losing enteropathy.