: WDFY3 (MIM#617485) defects may manifest neurodevelopmental disorders (NDDs) and opposite effects on brain size based on allelic effect. This case highlights a heterozygous WDFY3 nonsense variant linked to mild-to-moderate NDDs, macrocephaly, and unique facial features. Findings emphasize the importance of exome sequencing in NDDs for accurate diagnosis and clinical management.

Graziani, L., Carriero, M.l., Ferradini, V., Conte, C., Bengala, M., Sangiuolo, F.c., et al. (2025). WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and Macrocephaly. CLINICAL GENETICS, 107(3), 369-370 [10.1111/cge.14665].

WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and Macrocephaly

Graziani L.;Carriero M. L.;Ferradini V.;Sangiuolo F. C.;Novelli G.
2025-01-01

Abstract

: WDFY3 (MIM#617485) defects may manifest neurodevelopmental disorders (NDDs) and opposite effects on brain size based on allelic effect. This case highlights a heterozygous WDFY3 nonsense variant linked to mild-to-moderate NDDs, macrocephaly, and unique facial features. Findings emphasize the importance of exome sequencing in NDDs for accurate diagnosis and clinical management.
2025
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/03
Settore MEDS-01/A - Genetica medica
English
WDFY3
exome sequencing
haploinsufficiency
macrocephaly
neurodevelopmental disorders
Graziani, L., Carriero, M.l., Ferradini, V., Conte, C., Bengala, M., Sangiuolo, F.c., et al. (2025). WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and Macrocephaly. CLINICAL GENETICS, 107(3), 369-370 [10.1111/cge.14665].
Graziani, L; Carriero, Ml; Ferradini, V; Conte, C; Bengala, M; Sangiuolo, Fc; Novelli, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/417406
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