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Author

Bruna Fagundes Rodrigues Alaite

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Case report Open access Oct 2026

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

Van Maldergem syndrome (VMLDS) is an ultra-rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes. Fewer than 20 molecularly confirmed cases of VMLDS have bee...

Gabriela Roldão Correia-Costa, Bruna Fagundes Rodrigues Alaite, V. L. Gil-da-Silva-Lopes et al. · 0 citations

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