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PEMPix 2024 Online Case #4: Frozen Ever After

PEMBlog

Infants whose mothers received regular prenatal care are unlikely to develop congenital syphilis as it is routinely screened for during pregnancy. Infantile cortical hyperostosis, also known as Caffey’s disease, is an autosomal dominant genetic condition linked to a mutation in the COL1A1 gene which encodes type I collagen. Mäkitie, O.,

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Episode 213: Antiracism in Medicine Series – Episode 13 – Centering Asian Americans: Racism, Violence, and Health

The Clinical Problem Solvers

Effect of a media intervention on hepatitis B screening among Vietnamese Americans. [link] CPSolvers: Anti-Racism in Medicine Series Episode 13: Centering Asian Americans: Racism, Violence, and Health Show Notes by Naomi F. By appreciating the impact of factors affecting entire communities, we can be better positioned to act upon them.