Psychiatric manifestations of 22q11.2 deletion syndrome: A literature review

M. Bertrán, F. P. Tagle, M. Irarrázaval

Resultado de la investigación: Contribución a una revistaArtículo

5 Citas (Scopus)

Resumen

Introduction: The 22q11.2 deletion syndrome is a genetic disorder with variable clinical manifestations. It affects one out of 5950 neonates and has an autosomal dominant inheritance pattern. The aim of this article is to review its psychiatric manifestations and any underlying genetic alterations. Methods: We reviewed the scientific literature available as of October 2014 in the LILACS and Medline databases. Results: Sixty per cent of these patients fulfilled diagnostic criteria for a mental disorder at some point in their lives, referring to psychotic disorders, attention deficit hyperactivity disorder, mood disorders, anxiety disorders, and autism spectrum disorders. Specific genes, such as COMT and PRODH, have been linked to these psychiatric manifestations. Conclusions: It is necessary to raise awareness among all health care professionals so that they understand the relevance of these manifestations, are able to anticipate them, and can provide appropriate information to patients and family members.

Idioma originalEspañol
PublicaciónNeurologia
DOI
EstadoEn prensa - 18 ene 2015
Publicado de forma externa

Palabras clave

  • 22q11.2 deletion syndrome
  • Genetics
  • Psychiatric comorbidity

Áreas temáticas de ASJC Scopus

  • Neurología clínica

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