lymphoproliferative syndrome - перевод на арабский
Diclib.com
Словарь ChatGPT
Введите слово или словосочетание на любом языке 👆
Язык:

Перевод и анализ слов искусственным интеллектом ChatGPT

На этой странице Вы можете получить подробный анализ слова или словосочетания, произведенный с помощью лучшей на сегодняшний день технологии искусственного интеллекта:

  • как употребляется слово
  • частота употребления
  • используется оно чаще в устной или письменной речи
  • варианты перевода слова
  • примеры употребления (несколько фраз с переводом)
  • этимология

lymphoproliferative syndrome - перевод на арабский

PRIMARY IMMUNODEFICIENCY DISEASE CHARACTERIZED BY IMMUNE DYSREGULATION TYPICALLY AFTER VIRAL INFECTION, USUALLY ASSOCIATED WITH EPSTEIN-BARR VIRAL INFECTION
Lymphoproliferative; Lymphoproliferative disorder; Immunoproliferative diseases; Lymphoproliferative disease; Lymphoproliferative diseases; B-cell lymphoproliferative disease

lymphoproliferative syndrome      
‎ المُتَلاَزِمَةُ التَّكاثُرِيَّةُ اللِّمْفِيَّة‎
lymphoproliferative         
تَكاثُرِيٌّ لِمْفِيّ
lymphoproliferative         
‎ تَكاثُرِيٌّ لِمْفِيّ‎

Определение

Reye's syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.

Википедия

Lymphoproliferative disorders

Lymphoproliferative disorders (LPDs) refer to a specific class of diagnoses, comprising a group of several conditions, in which lymphocytes are produced in excessive quantities. These disorders primarily present in patients who have a compromised immune system. Due to this factor, there are instances of these conditions being equated with "immunoproliferative disorders"; although, in terms of nomenclature, lymphoproliferative disorders are a subclass of immunoproliferative disorders—along with hypergammaglobulinemia and paraproteinemias.

Примеры употребления для lymphoproliferative syndrome
1. Nathan Hartley, 13, and his three brothers Joshua, 14, Daniel, 10, and Luke, six, were diagnosed with the extremely rare genetic defect known as X–linked lymphoproliferative syndrome, or Duncan‘s syndrome, in November 2003.