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Harris, Susan R.
American journal of medical genetics. Part A, April 2024, 2024-Apr, 2024-04-00, Volume: 194, Issue: 4Journal Article
Marshall syndrome is an extremely rare genetic disorder usually diagnosed in infancy with a prevalence of <1 in 1 million. Based on the literature reviewed, this is the first case report to provide a longitudinal history of a child with Marshall syndrome (from birth to age 12.5 years). This longitudinal case report arose in part from desires of this child's parents to share the story of their early fears at her initial diagnosis and compare those to how well she has turned out.
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