Associated Papers
Prenatal Diagnosis of a Feingold Syndrome Pregnancy Complicated with Severe Preeclampsia: A Report of a Challenging Case.
Samara AA et al.
Genes, 2026
Rare features in Feingold syndrome type 1.
Ferroul F et al.
European Journal of Medical Genetics, 2025
A new variant of MYCN gene as a cause of Feingold syndrome.
Zeka N et al.
Clinical Case Reports, 2022
A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1.
Peleg A et al.
Clinical Dysmorphology, 2021
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