Coexistence of Neurofibromatosis Type 1 and Marfan Syndrome in a 13-Year-Old Boy: A Case Report

04 August 2026 : Case report Poland

Challenging differential diagnosis, Rare coexistence of disease or pathology

Piotr Wieniawski

^{ABDEFG 1*}, Magdalena Warych

^{BDEF 1}, Beata Kucińska

^{DEF 1}, Izabela Janiec^{CF 1}, Bożena Werner

^{DEF 1}

DOI: 10.12659/AJCR.950868

Am J Case Rep 2026; 27:e950868

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Introduction Case Report Discussion Conclusions References

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Figure 1 (A) Foot deformities. (B) Hand deformities, including arachnodactyly and phalangeal hypoplasia, characteristic of Marfan syndrome.

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