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- W3195536570 abstract "Primary microcephaly (PM) is defined as a significant reduction in occipitofrontal circumference (OFC) of prenatal onset. Clinical and genetic heterogeneity of PM represents a diagnostic challenge.We performed detailed phenotypic and genomic analyses in a large cohort (n = 169) of patients referred for PM and could establish a molecular diagnosis in 38 patients.Pathogenic variants in ASPM and WDR62 were the most frequent causes in non-consanguineous patients in our cohort. In consanguineous patients, microarray and targeted gene panel analyses reached a diagnostic yield of 67%, which contrasts with a much lower rate in non-consanguineous patients (9%). Our series includes 11 novel pathogenic variants and we identify novel candidate genes including IGF2BP3 and DNAH2. We confirm the progression of microcephaly over time in affected children. Epilepsy was an important associated feature in our PM cohort, affecting 34% of patients with a molecular confirmation of the PM diagnosis, with various degrees of severity and seizure types.Our findings will help to prioritize genomic investigations, accelerate molecular diagnoses, and improve the management of PM patients." @default.
- W3195536570 created "2021-08-30" @default.
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- W3195536570 date "2021-08-17" @default.
- W3195536570 modified "2023-10-14" @default.
- W3195536570 title "Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy" @default.
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