Barely Significant
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Neonatal Marfan syndrome: a case report of a novel fibrillin 1 mutation, with genotype-phenotype correlation and brief review of the literature.

Ital J Pediatr · 2024 · PMC11411867 · PMID 39294662

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quite significantno p-value reported
The extent of musculoskeletal disease is quite significant in older patients with Marfan syndrome: scoliosis, pectus deformity, and deformity of the foot.

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