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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Detalhes bibliográficos
Publicado no:BMC Psychiatry
Main Authors: GAULD, Christophe, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien, DEMILY, Caroline
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8285776/
https://ncbi.nlm.nih.gov/pubmed/34273950
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12888-021-03342-8
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