Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: 'Awareness to Act'.

Carrion, Prescilla; Semaka, Alicia; Batallones, Rolan; Slomp, Caitlin; Morris, Emily; Inglis, Angela; Moretti, Marlene; Austin, Jehannine

Carrion, Prescilla; Semaka, Alicia; Batallones, Rolan; Slomp, Caitlin; Morris, Emily; Inglis, Angela; Moretti, Marlene; Austin, Jehannine.

Afiliação

Carrion P; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Semaka A; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Batallones R; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Slomp C; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Morris E; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Inglis A; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Moretti M; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Austin J; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

J Genet Couns ; 31(1): 140-152, 2022 02.

Article em En | MEDLINE | ID: mdl-34224608

Assuntos

Síndrome de DiGeorge; Transtornos Psicóticos; Ansiedade; Criança; Síndrome de DiGeorge/epidemiologia; Síndrome de DiGeorge/genética; Síndrome de DiGeorge/terapia; Aconselhamento Genético; Humanos; Pais/psicologia

Palavras-chave

22q11.2 deletion; genetic counseling; intervention; mental health; psychiatric illness; velocardiofacial syndrome

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Síndrome de DiGeorge Tipo de estudo: Guideline / Qualitative_research Limite: Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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