Abstract
Alpha-1 antitrypsin deficiency (DAAT) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis, and, rarely, as the skin disease panniculitis [1], but other rare skin manifestations had been described previously in literature [2]. Despite being one of the most frequent genetic diseases, professionals need high clinical suspicion for its diagnosis.
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Schedule a callMore From: Journal of Clinical Microbiology and Biochemical Technology
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