Alpha-1 Detection Resources
Alpha-1 deficiency is a serious hereditary condition that is frequently underrecognized or misdiagnosed. According to a survey by Campos et al (2005) of 1,020 patients with Alpha-1 deficiency, the disease has taken an average of 8.3 years to diagnose from symptom onset. One-third of patients saw more than 2 physicians before being diagnosed.1
To facilitate the diagnosis and treatment of alpha-1 deficiency, CSL Behring is pleased to offer the Making a Clear Diagnosis brochure.

| An informative brochure that:
- Describes the clinical manifestations of Alpha-1 deficiency
- Presents guidelines for screening and testing your COPD patients for Alpha-1 deficiency and for counseling and treating patients with Alpha-1 deficiency.
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Proper diagnosis can make a real difference in the lives of patients and their families. Join us in helping reduce the time to diagnosis for Alpha-1 deficiency, to ensure patients receive treatment as soon as possible.
Call your local CSL Behring representative today to request this brochure and other detection resources. To get the name of your CSL Behring representative, please call 1-866-ZEMAIRA (1-866-936-2472).
CSL Behring and our predecessor companies have a long history of commitment to education and support for our physician and patient communities. We are proud to offer our services and be at your disposal as an ongoing resource, an advisor, and provide educational support to help make your diagnostic practices easier.
- Campos MA, Wanner A, Zhang G, Sandhaus RA. Chest. 2005;128(3):1179-1186.