Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review

BACKGROUND: Pathogenic variants of the AUTS2 (Autism Susceptibility candidate 2) gene predispose to intellectual disability, autism spectrum disorder, attention deficit hyperactivity disorder, facial dysmorphism and short stature. This phenotype is therefore associated with neurocognitive disturbanc...

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Detalles Bibliográficos
Autores principales: GAULD, Christophe, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien, DEMILY, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285776/
https://www.ncbi.nlm.nih.gov/pubmed/34273950
http://dx.doi.org/10.1186/s12888-021-03342-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285776/
https://www.ncbi.nlm.nih.gov/pubmed/34273950
http://dx.doi.org/10.1186/s12888-021-03342-8

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