Pedi Derm Education: Albinism Cases in Tanzania

Join Dr. Alanna Bree, Pediatric Dermatologist and Host of the Sagis Pedi Derm Education Series, as she shares compelling pediatric dermatology cases during Albinism Awareness Month. Explore the complexities of albinism that Dr. Bree encountered during her mission trip to Tanzania.

In this video, we’ll explore:

Understanding Oculocutaneous Albinism (OCA):

• Genetic Spectrum: A high-level overview of the different genetic types of OCA (e.g., OCA1, OCA2, OCA3, OCA4, OCA5, OCA6, OCA7) and the genes involved.
• Clinical Distinctions: Key differences in how each type presents in terms of skin, hair, and eye pigmentation, and associated visual impairments.

Beyond Pigmentation: Syndromic Forms of Albinism:

• Systemic Implications: An introduction to albinism as part of broader syndromes, impacting multiple body systems.
• Key Syndromes: High-level details on Hermansky-Pudlak Syndrome (HPS), Chediak-Higashi Syndrome (CHS), and albinism-like presentations in Angelman Syndrome (AS) and Prader-Willi Syndrome (PWS), as well as Ocular Albinism (OA).

In this video, you’ll learn:

• The diverse genetic and clinical presentations of various albinism types.
• How to differentiate between non-syndromic and syndromic forms of albinism.
• The importance of comprehensive understanding for accurate diagnosis and patient care.
• Insights relevant to global health contexts where specific challenges for Persons with Albinism exist.

Whether you’re a dermatology resident, a physician expanding your knowledge, or simply curious about inherited pigmentary disorders, this presentation offers powerful insights into the complexities of albinism.