hypofibrinogenemia

hypofibrinogenemia
Abnormally low concentration of fibrinogen in the circulating blood plasma.

* * *

hy·po·fi·brin·o·gen·emia or chiefly Brit hy·po·fi·brin·o·gen·ae·mia -fī-.brin-ə-jə-'nē-mē-ə n an abnormal deficiency of fibrinogen in the blood
hy·po·fi·brin·o·gen·emic or chiefly Brit hy·po·fi·brin·o·gen·ae·mic -'nē-mik adj

* * *

hy·po·fi·brin·o·gen·emia (hi″po-fi-brin″o-jə-neґme-ə) abnormally low levels of fibrinogen in the blood; called also fibrinogenopenia.

Medical dictionary. 2011.

Игры ⚽ Поможем написать реферат

Look at other dictionaries:

  • hypofibrinogenemia — hypofibrinogenemia. См. гипофибриногенемия. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • hypofibrinogenemia — n. fibrinogenopenia, fibrinogen in levels below normal in the blood, very low levels of fibrinogen in the blood, decrease in the concentration of fibrinogen in the blood …   English contemporary dictionary

  • гипофибриногенемия — hypofibrinogenemia гипофибриногенемия. НЗЧ, геморрагический диатез; характеризуется дефицитом фактора I свертывания крови (фибриноген); наследуется по аутосомно рецессивному типу, кластер генов F1 локализован на участке q28 хромосомы 4. (Источник …   Молекулярная биология и генетика. Толковый словарь.

  • afibrinogenemia — The absence of fibrinogen in the plasma. SEE ALSO: hypofibrinogenemia. congenital a. [MIM*202400] a rare disorder of blood coagulation in which little or no fibrinogen can be found in plasma because of a mutant …   Medical dictionary

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… …   Wikipedia

  • Bothrops — Taxobox name = Bothrops image caption = Common lancehead, B. atrox regnum = Animalia phylum = Chordata subphylum = Vertebrata classis = Reptilia ordo = Squamata subordo = Serpentes familia = Viperidae subfamilia = Crotalinae genus = Bothrops… …   Wikipedia

  • Waldenström's macroglobulinemia — DiseaseDisorder infobox Name = Waldenström s macroglobulinemia ICD10 = ICD10|C|88|0|c|81 ICDO = ICDO|9761|3 ICD9 = ICD9|273.3 OMIM = 153600 MedlinePlus = 000588 eMedicineSubj = med eMedicineTopic = 2395 DiseasesDB = 14030 MeshID = D008258… …   Wikipedia

  • Macrophage-activation syndrome — (MAS) is a severe, potentially life threatening, complication of several chronic rheumatic diseases of childhood. It occurs most commonly with systemic onset juvenile idiopathic arthritis (SoJIA), which is also known as Still s disease. In… …   Wikipedia

  • Thrombin clotting time — The Thrombin Clotting Time (TCT), also known as the Thrombin Time (TT), is a coagulation assay which is usually performed in order to detect for the therapeutic level of the anticoagulant Heparin. It is also sensitive in detecting the presence of …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”