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Alpha-1 Antitrypsin Deficiency
Alpha-1 antitrypsin deficiency is a genetic disorder characterized by a lack of protein, which leads to an increased risk of developing lung and liver diseases.
Alpha-1 Antitrypsin Deficiency in Pediatric Liver Disease (AATD) - A Complete Guide
Alpha-1 antitrypsin deficiency (AATD) in pediatric liver disease, highlights the genetic nature of the disorder and its impact on liver function.
Lab Tests for Alpha-1 Antitrypsin Deficiency - An Overview
Alpha-1 antitrypsin deficiency causes lung and liver problems. Prompt action and diagnosis prevent many complications.
Navigating the Challenges of Pediatric Alpha - 1 Antitrypsin Deficiency
It is a condition in pediatric patients known to be an inherited genetic disease that can cause damage to the tissues in the liver or lungs.
Alpha-1 Antitrypsin Deficiency - Causes, Symptoms, Diagnosis, and Treatment
Alpha-1 antitrypsin deficiency is an inherited disorder affecting the lungs, liver, and skin. The causes, symptoms, and treatment are explained in the article.
Smart Insulin Patches: Technical Breakthrough in Diabetes
Smart insulin patches are revolutionary insulin administrators that change the experience of diabetes care. Read more»Probiotics in Nonalcoholic Fatty Liver Disease (NAFLD) - Prevention and Management
The gut microbiome is closely linked to the development of NAFLD. In NAFLD cases, probiotic therapy regulates liver function, insulin, and lipid levels. Read more»Effective Strategies for Managing Anterior Epistaxis in Older Adults
Epistaxis or nosebleeds can be prevented through humidifiers, Aspirin, decongestants, and avoiding nose trauma. Read more»