Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders

Front Neurol. 2021 Jul 22:12:711288. doi: 10.3389/fneur.2021.711288. eCollection 2021.

Authors

Francesca Cogliati¹, Francesca Forzano², Silvia Russo¹

Affiliations

¹ Research Laboratory of Medical Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milan, Italy.
² Clinical Genetics Department, Guy's & St Thomas' National Health System Foundation Trust, London, United Kingdom.

No abstract available

Keywords: MRD23 syndrome; POLR3A; SETBP1 gene; SETD5 gene; microcephaly; overlapping phenotypes; pleiotropy of a single gene; ring20.

Publication types

Editorial