PEMPix 2024 Online Case #4: Frozen Ever After
PEMBlog
SEPTEMBER 26, 2024
Syphilis Complicating Pregnancy and Congenital Syphilis. 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. It causes changes in bones which typically begin in infancy and self-resolve by two years of age.
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