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Congenital Afibrinogenemia - Symptoms, Causes, Treatment
https://rarediseases.org/rare-diseases/afibrinogenemia-congenital/
WEBApr 24, 2023 · Congenital afibrinogenemia is a rare bleeding disorder characterized by absence of fibrinogen (also known as coagulation factor I) in the blood, a protein that is essential in the blood clotting (coagulation) process. Affected individuals may be susceptible to severe bleeding (hemorrhaging) episodes, particularly during infancy and childhood.
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Afibrinogenemia - National Organization for Rare Disorders
https://rarediseases.org/gard-rare-disease/afibrinogenemia/
WEBDisease Overview. Afibrinogenemia, sometimes called congenital afibrinogenemia, is an inherited blood disorder in which the blood does not clot normally. It occurs when there is a lack (deficiency) of a protein called fibrinogen (or coagulation factor I), which is needed for the blood to clot. [1413] [1414] Affected individuals may be ...
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Congenital afibrinogenemia - Wikipedia
https://en.wikipedia.org/wiki/Congenital_afibrinogenemia
WEBCongenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder.
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Familial afibrinogenemia - About the Disease - Genetic and Rare
https://rarediseases.info.nih.gov/diseases/5761/familial-afibrinogenemia/
WEBSummary. Afibrinogenemia, sometimes called congenital Afibrinogenemia, is an inherited blood disorder in which the blood does not clot normally. It occurs when there is a lack (deficiency) of a protein called fibrinogen (or coagulation factor I), …
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Afibrinogenemia: A Rare, Often Overlooked Bleeding Disorder
https://ashpublications.org/ashclinicalnews/news/5756/Afibrinogenemia-A-Rare-Often-Overlooked-Bleeding
WEBAfibrinogenemia is a very rare, inherited blood disorder in which the blood does not clot normally because of a mutation that leads to the absence of fibrinogen (also called coagulation factor I). Fibrinogen has a multitude of functions, including fibrin clot formation, platelet aggregation, and promoting wound healing at a site of injury.
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Factor I Deficiency, Fibrinogen Disorder, Afibrinogenemia
https://www.hemophilia.org/bleeding-disorders-a-z/types/other-factor-deficiencies/factor-i
WEBAfibrinogenemia and hypofibrinogenemia are usually diagnosed in newborns who exhibit excessive bleeding from the umbilical cord and after circumcision. Easy bruising, nose and mouth bleeds, and soft tissue bleeds are common. Joint and muscle bleeds can also occur.
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Afibrinogenemia - an overview | ScienceDirect Topics
https://www.sciencedirect.com/topics/medicine-and-dentistry/afibrinogenemia
WEBAfibrinogenemia and hypofibrinogenemia are the homozygous and heterozygous presentations of decreased fibrinogen synthesis (al-Mondhiry and Ehmann 1994 ). The clinical presentation for afibrinogenemia patients is with a bleeding disorder comparable to moderate or severe hemophilia.
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Congenital afibrinogenemia: MedlinePlus Genetics
https://medlineplus.gov/genetics/condition/congenital-afibrinogenemia/
WEBDescription. Congenital afibrinogenemia is a bleeding disorder caused by impairment of the blood clotting process. Normally, blood clots protect the body after an injury by sealing off damaged blood vessels and preventing further blood loss. However, bleeding is uncontrolled in people with congenital afibrinogenemia.
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Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622093/
WEBNov 19, 2021 · Afibrinogenemia and hypofibrinogenemia are the consequence of mutations in the homozygous, heterozygous, or compound heterozygous state in one of three genes encoding the fibrinogen chains, which can affect the synthesis, assembly, intracellular processing, stability, or secretion of fibrinogen.
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Congenital afibrinogenemia Information | Mount Sinai - New York
https://www.mountsinai.org/health-library/diseases-conditions/congenital-afibrinogenemia
WEBCongenital afibrinogenemia. Afibrinogenemia; Hypofibrinogenemia; Dysfibrinogenemia; Factor I deficiency. Congenital fibrinogen deficiency is a very rare, inherited blood disorder in which the blood does not clot normally. It affects a protein called fibrinogen. This protein is needed for the blood to clot. Causes.
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