"Afibrinogenemia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A deficiency or absence of FIBRINOGEN in the blood.
| Descriptor ID |
D000347
|
| MeSH Number(s) |
C15.378.100.100.056 C15.378.100.141.072 C15.378.463.067 C16.320.099.056
|
| Concept/Terms |
Afibrinogenemia- Afibrinogenemia
- Afibrinogenemias
- Fibrinogen Deficiency
- Deficiency, Fibrinogen
- Fibrinogen Deficiencies
Congenital Afibrinogenemia- Congenital Afibrinogenemia
- Afibrinogenemia, Congenital
- Afibrinogenemias, Congenital
- Congenital Afibrinogenemias
- Familial Afibrinogenemia
- Afibrinogenemia, Familial
- Afibrinogenemias, Familial
- Familial Afibrinogenemias
- Congenital Afibrinogenaemia
- Afibrinogenaemia, Congenital
- Afibrinogenaemias, Congenital
- Congenital Afibrinogenaemias
- Hypofibrinogenemia, Congenital
- Congenital Hypofibrinogenemia
- Congenital Hypofibrinogenemias
- Hypofibrinogenemias, Congenital
|
Below are MeSH descriptors whose meaning is more general than "Afibrinogenemia".
Below are MeSH descriptors whose meaning is more specific than "Afibrinogenemia".
This graph shows the total number of publications written about "Afibrinogenemia" by people in this website by year, and whether "Afibrinogenemia" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Afibrinogenemia" by people in Profiles.
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Blood, Sweat, and Fears: A Novel Mutation Associated With Anaphylaxis and Nonresponse in a Patient With Afibrinogenemia. J Pediatr Hematol Oncol. 2021 03 01; 43(2):e260-e263.
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Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype. Pediatr Blood Cancer. 2021 03; 68(3):e28713.
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An infant with a diagnostically challenging hepatic teratoma, hypofibrinogenemia, and adrenal neuroblastoma: case report. Pediatr Dev Pathol. 2015 May-Jun; 18(3):251-6.
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Hypofibrinogenemia, dysfibrinogenemia or hypodysfibrinogenemia?: comment on 'The dilemma of inherited dysfibrinogenemia during pregnancy'. Blood Coagul Fibrinolysis. 2013 Apr; 24(3):353-4.
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Use of purified fibrinogen concentrate for dysfibrinogenemia and importance of laboratory fibrinogen activity measurement. Pediatr Blood Cancer. 2013 Mar; 60(3):500-2.
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Hypodysfibrinogenemia during pregnancy, labor, and delivery. Obstet Gynecol. 2003 May; 101(5 Pt 2):1092-4.
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Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia. Hepatology. 2002 Sep; 36(3):652-8.