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Original Question

This study aims to identify the areas where the underdiagnosis of Alpha-1 Antitrypsin deficiency occurs and to highlight the significant changes needed within medical services to address these challenges. Biological inheritance plays a crucial role in the diagnosis of Alpha-1, and improvements can be made to address any gaps in the diagnostic process. This situation presents a valuable opportunity for the medical community to contribute to a more effective and comprehensive diagnostic approach. The literature review section of this paper will explore the barriers currently hindering progress while also suggesting areas for improvement in testing, augmentation therapy, early indicators of COPD, and the relationship between smoking and Alpha-1 Antitrypsin deficiency. Keywords: Augmentation therapy, alpha-1 antitrypsin deficiency, chronic obstructive pulmonary disease, tobacco smoking, testing alpha-1, biological inheritance, genetic disorder, diagnosis, management, liver damage, server alpha-1, lung cancer, immunology, liver function. Questions: How this project might apply to Medical laboratory Science as discipline. If you were to take this project a step further, what would you recommend? After viewing this presentation, I was left wondering…

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