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.· American Journal of Medical...· 0 citations
Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%-5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce i...
Gabriela Roldão Correia-Costa, J. R. M. Prota, A. Marques-de-Faria et al.· American Journal of Medical...· 0 citations
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