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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Dades bibliogràfiques
Publicat a:BMC Psychiatry
Autors principals: GAULD, Christophe, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien, DEMILY, Caroline
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2021
Matèries:
Case Report
Accés en línia: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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