agammaglobulinemia in English
Use "agammaglobulinemia" in a sentence
1. X-linked Agammaglobulinemia, also called Bruton's Agammaglobulinemia or congenital Agammaglobulinemia, was the first immunodeficiency disease ever identified
2. The most common form of Agammaglobulinemia is X-linked Agammaglobulinemia (AGMX1
3. X-linked Agammaglobulinemia, also called Bruton's Agammaglobulinemia or congenital Agammaglobulinemia, was the first immunodeficiency disease ever identified
4. X-linked Agammaglobulinemia, also called Bruton's Agammaglobulinemia or congenital Agammaglobulinemia, was the first immunodeficiency disease ever identified
5. Agammaglobulinemia can be categorized into the following types: Early-onset Bruton’s Agammaglobulinemia (X-Linked Agammaglobulinemia or XLA) Early-onset Agammaglobulinemia not due to Bruton’s Adult-onset common variable immunodeficiency; Bruton’s Agammaglobulinemia is the most common cause of Agammaglobulinemia, especially in children.
6. Agammaglobulinemia definition: 1
7. Autosomal recessive Agammaglobulinemia (Swiss type) X-linked Agammaglobulinemia [Bruton] (with growth hormone deficiency)
8. También es llamada Agammaglobulinemia de Bruton o Agammaglobulinemia congénita
9. Agammaglobulinemia, also known as Bruton Agammaglobulinemia, X-linked Agammaglobulinemia (XLA), or Bruton tyrosine kinase (BTK) deficiency, is a primary immunodeficiency characterized by recurrent bacterial infections in affected males
10. How to use Agammaglobulinemia in a sentence.
11. This disease, sometimes called Bruton’s Agammaglobulinemia or Congenital Agammaglobulinemia, was one of the first immunodeficiency diseases to be identified
12. Agammaglobulinemia agammaglobulinemias agammaglobulinemic backgrounding beglamouring bludgeoning Boguing bourgeoisifying
13. Also known as Bruton's Agammaglobulinemia or congenital Agammaglobulinemia, X-Linked Agammaglobulinemia is an inherited disorder, occurring mainly in boys, in which your child is unable to produce antibodies (the body's primary defense against bacteria and viruses)
14. Agammaglobulinemia, a genetic autoimmune disorder, is an inherited immune system disorder in which the body’s immune system is not able to make enough antibodies to fight off infections either bacteria or viral.Agammaglobulinemia is also known by the name of Bruton’s Agammaglobulinemia or X-linked Agammaglobulinemia
15. X-Linked Agammaglobulinemia (XLA) was first described in 1952 by Dr
16. Bruton Agammaglobulinemia or X-linked Agammaglobulinemia (XLA) is an inherited immunodeficiency disorder characterized by the absence of mature B cells, resulting in severe antibody deficiency and recurrent infections
17. Agammaglobulinemia, non-Bruton type is a rare form of Agammaglobulinemia, which is a primary immunodeficiency characterized by very low levels of immunoglobulins (proteins made by the immune system to help fight infections)
18. La Agammaglobulinemia es hereditaria, lo cual significa que otras personas en la familia pueden padecerla
19. Infants with X-linked Agammaglobulinemia start having recurring coughs and/or infections of the nose
20. Agammaglobulinemia definition is - a condition in which the body forms few or no gamma globulins or antibodies
21. Agammaglobulinemia, or hypogammaglobulinemia, is the most common of the primary immunodeficiencies, accounting for approximately 50% of cases
22. Agammaglobulinemia is a form of primary immunodeficiency demarcated by defects in B-cell function due to gene mutations encoding the Bruton tyrosine kinase protein on chromosome X, which is why the term X-linked Agammaglobulinemia is used in the literature
23. The condition described in this landmark article is now referred to as Bruton's or X-linked Agammaglobulinemia (XLA)
24. Resulting in Agammaglobulinemia leading to particular susceptibility to bacterial infections of the respiratory and digestive tracts
25. Congenital Agammaglobulinemia is a rare condition, occurring in males, and resulting in decreased or absent production of antibodies
26. Agammaglobulinemia, or hypogammaglobulinemia, is the most common of the primary immunodeficiencies, accounting for approximately 50% of cases
27. Children with X-linked Agammaglobulinemia should not receive live viral vaccines such as the live polio vaccine
28. Agammaglobulinemia, or hypogammaglobulinemia, is the most common of the primary immunodeficiencies, accounting for approximately 50% of cases
29. X-linked Agammaglobulinemia is a hereditary immunodeficiency disorder due to a mutation in a gene on the X (sex) chromosome
30. X-linked Agammaglobulinemia is a hereditary immunodeficiency disorder due to a mutation in a gene on the X (sex) chromosome
31. X-linked Agammaglobulinemia (XLA) is characterized by recurrent bacterial infections in affected males in the first two years of life
32. X-linked Agammaglobulinemia More often , hypogammaglobulinemia develops as a result of another condition, called secondary or acquired immune deficiencies
33. Agammaglobulinemia is an inherited disorder in which a person has very low levels of protective immune system proteins called immunoglobulins
34. Agammaglobulinemia [a″gam-ah-glob″u-lin-e´me-ah] absence or severe deficiency of the plasma protein gamma globulin
35. "X-linked" means that the gene which causes this Agammaglobulinemia is located on the X chromosome, and therefore only affects males
36. Frequently called Bruton's Agammaglobulinemia, XLA is caused by a genetic mistake in a gene called Bruton's tyrosine kinase (BTK), which prevents B cells from developing normally.
37. Acquired Agammaglobulinemia is secondary to other disorders and is usually a hypogammaglobulinemia, that is, a deficiency rather than total absence of this plasma protein
38. X-Linked Agammaglobulinemia (XLA) is an inherited immunodeficiency in which the body is unable to produce the antibodies needed to defend against bacteria and viruses
39. Agammaglobulinemia is an immune disorder related to antibody deficiency (hypogammaglobulinemia) and is manifested in a variety of immune deficiency disorders in which the immune system is compromised
40. Agammaglobulinemia is a primary immunodeficiency characterized by profoundly low or absent serum antibodies and low or absent circulating B cells due to an early block of B-cell development
41. Agammaglobulinemia is a rare form of primary immune deficiency characterized by absence of circulating B cells and low serum levels of all immunoglobulin classes, in the presence of normal T cell counts and function
42. "X-linked" means that the gene which causes this Agammaglobulinemia is located on the X chromosome, and therefore primarily affects males because it is unlikely that females will have two
43. "X-linked" means that the gene which causes this Agammaglobulinemia is located on the X chromosome, and therefore primarily affects males because it is unlikely that females will have two
44. X-linked Agammaglobulinemia (XLA), a more uncommon humoral immune defect than CVID, is due to an abnormality of an X chromosome–encoded B-cell cytoplasmic tyrosine kinase necessary for B-cell maturation (Conley et al., 1994)
45. "Ligada al cromosoma X" significa que el gen que produce la Agammaglobulinemia se ubica en el cromosoma X y, por lo tanto, afecta principalmente a los hombres debido a que solo tienen un cromosoma X
46. Agammaglobulinemia definition, a condition of the blood, either congenital or acquired, in which there is near or complete absence of gamma globulin and a failure of the body to form antibodies, resulting in a frequent occurrence of infectious disease
47. Diseases associated with Bmx include Agammaglobulinemia, X-Linked and Integrative Agnosia.Among its related pathways are Apoptotic cleavage of cellular proteins and PI Metabolism.Gene Ontology (GO) annotations related to this gene include transferase activity, transferring phosphorus-containing groups and protein tyrosine …
48. Results: We describe two patients with X-linked Agammaglobulinemia (XLA) aged 34 and 26 years with complete absence of B cells from peripheral blood who developed COVID-19, as diagnosed by SARS-CoV-2 detection by nasopharyngeal swab, while receiving immunoglobulin infusions
49. Agammaglobulinemia also known as hypogammaglobulinemia, is a group of rare inherited immune deficiencies characterized by a low concentration of antibodies in the blood due to the lack of particular lymphocytes in the blood and lymph 1).Antibodies are proteins (immunoglobulins, (IgM), (IgG) etc) that are critical and key components of the immune system.