alpha 1 antitrypsin deficiency | Alpha-1 Antitrypsin Deficiency: Cause

Keyword	CPC	PCC	Volume	Score	Length of keyword
alpha 1 antitrypsin deficiency	1.83	0.9	2444	92	30
alpha	1.35	0.6	8774	64	5
1	1.42	0.9	7438	98	1
antitrypsin	0.78	0.1	2817	40	11
deficiency	1.2	0.2	1091	41	10

Keyword	CPC	PCC	Volume	Score
alpha 1 antitrypsin deficiency	0.2	0.3	117	24
alpha 1 antitrypsin deficiency guidelines	0.56	0.4	9118	1
alpha 1 antitrypsin deficiency liver	0.96	0.7	9657	25
alpha 1 antitrypsin deficiency icd 10	1.75	0.3	1253	65
alpha 1 antitrypsin deficiency symptoms	0.82	0.3	8384	73
alpha 1 antitrypsin deficiency treatment	1.72	0.1	3319	89
alpha 1 antitrypsin deficiency nhs	0.57	0.8	5861	25
alpha 1 antitrypsin deficiency copd	0.92	0.4	7508	52
alpha 1 antitrypsin deficiency test	1.75	0.3	2125	60
alpha 1 antitrypsin deficiency inheritance	0.26	0.1	5047	43
alpha 1 antitrypsin deficiency radiology	0.66	0.6	8596	54
alpha 1 antitrypsin deficiency lung	2	0.1	1142	65
alpha 1 antitrypsin deficiency carrier	0.65	0.7	1172	53
alpha 1 antitrypsin deficiency emphysema	1.83	1	2707	28
alpha 1 antitrypsin deficiency uptodate	1.98	0.3	4046	49
alpha 1 antitrypsin deficiency prognosis	0.55	1	573	97
alpha 1 antitrypsin deficiency drugs	0.78	1	9771	91
alpha 1 antitrypsin deficiency diagnosis	0.63	0.6	3908	74
alpha 1 antitrypsin deficiency infusion	1.65	0.7	4952	26
alpha 1 antitrypsin deficiency genereviews	0.54	0.6	374	21
alpha 1 antitrypsin deficiency phenotype	2	0.3	3705	64

Search Results related to alpha 1 antitrypsin deficiency 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 …

DA: 48 PA: 34 MOZ Rank: 56

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, or an increased risk of …

DA: 25 PA: 52 MOZ Rank: 39

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: 66 PA: 45 MOZ Rank: 34

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: 80 PA: 82 MOZ Rank: 29

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: 74 PA: 85 MOZ Rank: 34

What is Alpha-1? - Alpha-1 Foundation
alpha1.org

https://alpha1.org/what-is-alpha1/

WEBThere is no cure for Alpha-1, but treatment can help people with Alpha-1 manage symptoms. Avoiding certain behaviors, like smoking, can help slow the progression of Alpha-1 lung disease. Read the What is Alpha-1? brochure to learn more. Watch the video: Alpha-1 Antitrypsin Deficiency – How It Works.

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About Alpha-1 Antitrypsin Deficiency - National Human Genome …
genome.gov

https://www.genome.gov/Genetic-Disorders/Alpha-1-Antitrypsin-Deficiency

WEBJan 4, 2012 · Alpha-1 antitrypsin deficiency (AATD) is an inherited condition that causes low levels of, or no, alpha-1 antitrypsin (AAT) in the blood. AATD occurs in approximately 1 in 2,500 individuals. This condition is found in all ethnic groups; however, it occurs most often in whites of European ancestry.

DA: 24 PA: 70 MOZ Rank: 53

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 deficiency is congenital lack of a primary lung antiprotease, alpha-1 antitrypsin, which leads to increased protease-mediated tissue destruction and emphysema in adults. Hepatic accumulation of abnormal alpha-1 antitrypsin can cause liver disease in both children and adults.

DA: 98 PA: 99 MOZ Rank: 47

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.

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