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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Vydáno v:BMC Psychiatry
Hlavní autoři: GAULD, Christophe, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien, DEMILY, Caroline
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2021
Témata:
Case Report
On-line přístup: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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