Results 171 to 180 of about 30,835,114 (202)
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Alpha-1-Antitrypsin Deficiency Panniculitis

Dermatologic Clinics, 2008
Alpha-1-antitrypsin deficiency is a congenital error of metabolism linked to pulmonary (emphysema) and liver (cirrhosis) disease. Since 1972, panniculitis has been associated with this deficiency, initially related to Weber-Christian syndrome and finally as a differentiated entity.
Ricardo, Valverde   +4 more
openaire   +2 more sources

Detecting Alpha-1 Antitrypsin Deficiency

Annals of the American Thoracic Society, 2016
Abstract Alpha-1 antitrypsin deficiency is a widely underrecognized condition, with evidence of persisting long diagnostic delays and patients’ frequent need to see multiple physicians before initial diagnosis. Reasons for underrecognition include inadequate understanding of alpha-1 antitrypsin deficiency by physicians and allied ...
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[Alpha 1-antitrypsin deficiency].

Revue des maladies respiratoires, 2016
Pulmonary emphysema and liver disease are the clinical expressions of alpha 1-antitrypsin deficiency, an autosomal recessive genetic disease.Alpha 1-antitrypsin deficiency is usually associated with the homozygous Z variant of the SERPINA1 gene.
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Alphain1-antitrypsin deficiency

Current Treatment Options in Gastroenterology, 2000
Most of the care of liver disease in alpha(1)-antitrypsin (alpha(1)-AT) deficiency involves supportive management for complications of chronic liver disease including gastrointestinal bleeding, ascites, edema, encephalopathy, coagulation disturbances, spontaneous bacterial peritonitis, and hepatorenal syndrome.
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Alpha-1-Antitrypsin Deficiency

Clinics in Chest Medicine, 1983
S, Idell, A B, Cohen
openaire   +3 more sources

MZ Alpha-1 Antitrypsin Deficiency

American Journal of Respiratory and Critical Care Medicine, 2022
Oliver J, McElvaney   +4 more
openaire   +2 more sources

Alpha-1 antitrypsin deficiency

The Nurse Practitioner, 2014
Cathy R, Kessenich, Kathryn, Bacher
openaire   +2 more sources

Alpha-1 antitrypsin deficiency

Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition caused by decreased plasma and tissue levels of alpha-1 antitrypsin (AAT) that can lead to serious lung and liver disease in children and adults. AATD patients face challenges such as under diagnosis, clinical variability, and limited treatment options for liver disease.
Andrea Briem-Richter   +2 more
openaire   +3 more sources

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