alpha 1 antitrypsin | Alpha-1 Antitrypsin Deficiency: Causes, Symptoms

Keyword	CPC	PCC	Volume	Score	Length of keyword
alpha 1 antitrypsin	1.06	0.2	3573	33	19
alpha	1.93	0.8	9452	15	5
1	0.2	0.3	5148	25	1
antitrypsin	0.41	0.9	2879	93	11

Keyword	CPC	PCC	Volume	Score
alpha 1 antitrypsin deficiency	0.22	0.6	7104	45
alpha 1 antitrypsin	1.79	0.9	8394	87
alpha 1 antitrypsin test	0.79	0.2	634	96
alpha 1 antitrypsin deficiency guidelines	0.73	0.5	4019	38
alpha 1 antitrypsin phenotype	0.02	0.2	7094	6
alpha 1 antitrypsin deficiency liver	0.51	0.4	9006	54
alpha 1 antitrypsin deficiency icd 10	1.35	1	2068	92
alpha 1 antitrypsin deficiency symptoms	0.05	0.5	3768	93
alpha 1 antitrypsin deficiency treatment	1.72	0.4	8179	67
alpha 1 antitrypsin deficiency nhs	1.33	0.5	5638	82
alpha 1 antitrypsin deficiency copd	1.81	0.7	7167	2
alpha 1 antitrypsin elevated	1.45	0.2	3891	11
alpha 1 antitrypsin function	0.28	0.9	8839	34
alpha 1 antitrypsin free test	0.38	1	1233	33
alpha 1 antitrypsin deficiency test	1.25	0.6	5715	12
alpha 1 antitrypsin deficiency inheritance	1.26	0.8	2166	76
alpha 1 antitrypsin deficiency radiology	0.5	0.1	9937	68
alpha 1 antitrypsin genotype test	1.93	0.2	217	66
alpha 1 antitrypsin pims phenotype	1.24	0.4	891	76
alpha 1 antitrypsin deficiency prognosis	1.73	0.9	1736	51
alpha 1 antitrypsin deficiency drugs	1.52	0.6	7497	35
alpha 1 antitrypsin deficiency infusion	1.1	0.2	1449	23
alpha 1 antitrypsin test cost	1.21	1	5749	52

Search Results related to alpha 1 antitrypsin on Search Engine

Alpha-1 Antitrypsin Deficiency: Causes, Symptoms & Treatment
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/21175-alpha-1-antitrypsin-deficiency

WEBOct 18, 2022 · Alpha-1 antitrypsin deficiency (sometimes just called “Alpha-1”) is an inherited genetic disorder that causes low levels of a protein (AAT) that protects your lungs. Alpha-1 increases your risk of developing certain diseases, including emphysema (damaged air sacs in your lungs), cirrhosis (liver scarring) and panniculitis (an uncommon skin ...

DA: 62 PA: 28 MOZ Rank: 32

Alpha-1 antitrypsin - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Alpha-1_antitrypsin

WEBAlpha-1 antitrypsin or α 1-antitrypsin (A1AT, α 1 AT, A1A, or AAT) is a protein belonging to the serpin superfamily. It is encoded in humans by the SERPINA1 gene. A protease inhibitor, it is also known as alpha 1 –proteinase inhibitor (A1PI) or alpha 1-antiproteinase (A1AP) because it inhibits various proteases (not just trypsin).

DA: 24 PA: 39 MOZ Rank: 83

Alpha-1 Antitrypsin Deficiency - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK442030/

WEBFeb 7, 2023 · Alpha-1 antitrypsin (AAT) deficiency is a clinically under-recognized genetic disorder that causes the defective production of alpha-1 antitrypsin protein. AAT protein protects the body from the neutrophil elastase enzyme, which is released from white blood cells to fight infection.

DA: 49 PA: 52 MOZ Rank: 71

COPD - Alpha-1 Antitrypsin Deficiency | NHLBI, NIH
nih.gov

https://www.nhlbi.nih.gov/health/alpha-1-antitrypsin-deficiency

WEBLast updated on October 25, 2023. Alpha-1 antitrypsin (AAT) deficiency increases an individual’s risk for COPD. The deficiency is an inherited genetic condition with no cure. The resulting COPD would be treated in the standard manner, with bronchodilators, steroids, pulmonary rehabilitation, oxygen therapy, and surgery.

DA: 24 PA: 79 MOZ Rank: 2

Alpha-1 antitrypsin deficiency: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/alpha-1-antitrypsin-deficiency/

WEBDescription. Alpha-1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease. The signs and symptoms of the condition and the age at which they appear vary among individuals. People with alpha-1 antitrypsin deficiency usually develop the first signs and symptoms of lung disease between ages 25 and 50.

DA: 17 PA: 76 MOZ Rank: 85

Alpha-1 antitrypsin deficiency - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Alpha-1_antitrypsin_deficiency

WEBAlpha-1 antitrypsin deficiency (A1AD or AATD) is a genetic disorder that may result in lung disease or liver disease. Onset of lung problems is typically between 20 and 50 years of age. This may result in shortness of breath, wheezing, …

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Alpha-1 Antitrypsin Deficiency - MedlinePlus
medlineplus.gov

https://medlineplus.gov/alpha1antitrypsindeficiency.html

WEBSep 19, 2023 · Alpha-1 antitrypsin deficiency (AAT deficiency, or AATD) is an inherited condition that raises your risk for lung and liver disease. If you have this condition, your body doesn't make enough alpha-1 antitrypsin (AAT). AAT is made by your liver.

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Alpha-1 Antitrypsin Deficiency - Pulmonary Disorders - Merck …
merckmanuals.com

https://www.merckmanuals.com/professional/pulmonary-disorders/chronic-obstructive-pulmonary-disease-and-related-disorders/alpha-1-antitrypsin-deficiency

WEBAlpha-1 antitrypsin is a neutrophil elastase inhibitor (an antiprotease), the major function of which is to protect the lungs from protease-mediated tissue destruction.

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Alpha-1 Antitrypsin Deficiency - Lung and Airway Disorders
merckmanuals.com

https://www.merckmanuals.com/home/lung-and-airway-disorders/chronic-obstructive-pulmonary-disease-copd/alpha-1-antitrypsin-deficiency

WEBAlpha-1 antitrypsin deficiency is a hereditary disorder in which a lack or low level of the enzyme alpha-1 antitrypsin damages the lungs and liver. Alpha-1 antitrypsin deficiency is caused by an inherited gene mutation. Infants may develop jaundice and liver damage. Cirrhosis can develop during childhood.

DA: 80 PA: 82 MOZ Rank: 70

Alpha 1 -Antitrypsin Deficiency - The New England Journal of Medicine
nejm.org

https://www.nejm.org/doi/full/10.1056/NEJMra1910234

WEBApr 8, 2020 · Alpha1-antitrypsin (AAT) deficiency is one of the most common genetic diseases. Most persons carry two copies of the wild-type M allele of SERPINA1, which encodes AAT, and have normal...

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