
Haemolytic uraemic syndrome - BMJ Best Practice
Jun 22, 2022 · Haemolytic uraemic syndrome (HUS) is characterised by the triad of microangiopathic haemolytic anaemia, thrombocytopenia, and acute kidney injury. Most cases of HUS occur in children and are diarrhoea-associated (D+ HUS).
Hemolytic uremic syndrome - Symptoms, diagnosis and treatment …
Jun 22, 2022 · Hemolytic uremic syndrome (HUS) is characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. Most cases of HUS occur in children and are diarrhea-associated (D+ HUS).
Hemolytic uremic syndrome - References | BMJ Best Practice US
Hemolytic uremic syndrome (HUS) is characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. Most cases of HUS occur in children and are diarrhea-associated (D+ HUS).
Thrombotic thrombocytopenic purpura - BMJ Best Practice
Mar 16, 2022 · Atypical hemolytic uremic syndrome (aHUS) is a complement-mediated microangiopathy which clinically may masquerade as TTP, but is due to abnormalities in complement regulation.
Thrombotic thrombocytopenic purpura - BMJ Best Practice
Mar 16, 2022 · Atypical haemolytic uraemic syndrome (aHUS) is a complement-mediated microangiopathy which clinically may masquerade as TTP, but is due to abnormalities in complement regulation. [1] [7] Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med. 2009;361:1676-1687. http://www.ncbi.nlm.nih.gov/pubmed/19846853?tool=bestpractice.com
Sintomas, diagnóstico e tratamento - BMJ Best Practice
A SHU atípica ocorre devido a anormalidades na via regulatória alternativa do complemento, resultando em dano celular endotelial e causando trombose microvascular. A SHU atípica pode ocorrer em adultos e crianças. [3] Yan K, Desai K, Gullapalli L, et al. Epidemiology of atypical hemolytic uremic syndrome: a systematic literature review.
Paroxysmal nocturnal hemoglobinuria - BMJ Best Practice
Mar 19, 2025 · Paroxysmal nocturnal hemoglobinuria (PNH) is a hemolytic anemia characterized by evidence of intravascular hemolysis such as hemoglobinuria and elevation of plasma lactate dehydrogenase. Diagnosis can be made by flow cytometry of granulocytes and red blood cells, looking for the lack of the glycosylphosphatidylinositol anchor or of proteins dependent on it for attachment to the cell membrane ...
Symptoms, diagnosis and treatment - BMJ Best Practice
Mar 11, 2025 · HELLP syndrome is considered to be a severe form of pre-eclampsia (sometimes called 'atypical pre-eclampsia') characterised by haemolysis (H), also expressed as microangiopathic haemolytic anaemia, elevated liver enzymes (EL), and low platelets (LP). The condition usually occurs antepartum, betwe...
Symptoms, diagnosis and treatment - BMJ Best Practice
Aug 6, 2024 · Hepatic encephalopathy is a neuropsychiatric syndrome caused by acute or chronic advanced hepatic insufficiency. Symptoms vary in severity from a mild alteration in mental state to coma but are often reversible with treatment. Causation is thought to be multi-factorial, resulting in brain exposure to ammonia that has bypassed the liver through portosystemic shunting. Diagnosis is …
ჰემოლიტიკური ურემიული სინდრომი - სიმპტომების, …
ჰემოლიზურ-ურემიული სინდრომი (HUS) ხასიათდება მიკროანგიოპათიური ჰემოლიზური ანემიის, თრომბოციტოპენიით და თირკმლის მწვავე ...