Add to ORKGPanniculitis is a recognized, but rare complication of α1-antitrypsin (A1AT) deficiency. Less than 60 cases have been reported, mostly in the homozygous PiZZ variant. We report the case of a 55-year old woman with A1AT panniculitis associated with the heterozygous phenotype PiMS and discrete reduction of A1AT serum levels. In addition, the pathophysiology of the disease, clinical and histopathological features, and current treatment possibilities are briefly reviewed
Alpha 1-antitrypsin (AAT) belongs to the family of serpins (serine protease inhibitors). Loop sheet ...
a1-Antitrypsin (a1AT) deficiency is an autosomal reces-sive disorder that can cause pulmonary emphys...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Panniculitis is a recognized, but rare complication of α1-antitrypsin (A1AT) deficiency. Less than 6...
Background: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitryps...
Abstract: Alpha-1-Antitrypsin (AAT) deficiency associated panniculitis is commonly included in the d...
SUMMARY A patient with a low serum concentration of a1-antitrypsin (0-1 g/l) but with an M-like phen...
Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which re...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
The deficiency of alpha-1 protease inhibitor, or alpha-1-antitrypsin (A1AT), predisposes to chronic ...
α1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading ...
Alpha-1 antitrypsin deficiency is an autosomal, codominant disorder caused by mutations of the SERPI...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
We describe the clinical presentation and outcome in a series of eight patients with systemic necrot...
Summary: We describe a case of the heterozygous antitrypsin phenotype IS. The 20 years old female em...
Alpha 1-antitrypsin (AAT) belongs to the family of serpins (serine protease inhibitors). Loop sheet ...
a1-Antitrypsin (a1AT) deficiency is an autosomal reces-sive disorder that can cause pulmonary emphys...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Panniculitis is a recognized, but rare complication of α1-antitrypsin (A1AT) deficiency. Less than 6...
Background: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitryps...
Abstract: Alpha-1-Antitrypsin (AAT) deficiency associated panniculitis is commonly included in the d...
SUMMARY A patient with a low serum concentration of a1-antitrypsin (0-1 g/l) but with an M-like phen...
Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which re...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
The deficiency of alpha-1 protease inhibitor, or alpha-1-antitrypsin (A1AT), predisposes to chronic ...
α1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading ...
Alpha-1 antitrypsin deficiency is an autosomal, codominant disorder caused by mutations of the SERPI...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
We describe the clinical presentation and outcome in a series of eight patients with systemic necrot...
Summary: We describe a case of the heterozygous antitrypsin phenotype IS. The 20 years old female em...
Alpha 1-antitrypsin (AAT) belongs to the family of serpins (serine protease inhibitors). Loop sheet ...
a1-Antitrypsin (a1AT) deficiency is an autosomal reces-sive disorder that can cause pulmonary emphys...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...