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Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation).
Yardeni, Maya; Weisman, Omri; Mandel, Hanna; Weinberger, Ronnie; Quarta, Giovanni; Salazar-Mendiguchía, Joel; Garcia-Pavia, Pablo; Lobato-Rodríguez, Maria José; Simon, Lourdes Fajardo; Dov, Freimark; Arad, Michael; Gothelf, Doron.
Afiliação
  • Yardeni M; The Behavioral Neurogenetics Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Weisman O; The Behavioral Neurogenetics Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Mandel H; Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
  • Weinberger R; Metabolic Unit, Children's Hospital, Rambam Health Care Campus, Technion-Israel Institute of Technology, Haifa, Israel.
  • Quarta G; The Behavioral Neurogenetics Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Salazar-Mendiguchía J; Cardiology Department ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Garcia-Pavia P; Cardiomyopathy Unit, Heart Failure and Transplant Program, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain.
  • Lobato-Rodríguez MJ; Health in Code, Cardiovascular Genetics, A Coruña, Spain.
  • Simon LF; Department of Cardiology, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
  • Dov F; Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
  • Arad M; Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
  • Gothelf D; Leviev Heart Center, Sheba Medical Center, Tel Hashomer, Israel.
Am J Med Genet A ; 173(9): 2461-2466, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28627787
ABSTRACT
Danon disease (DD) is a rare X-linked disorder caused by loss-of-function mutations in the LAMP2 gene, which encodes lysosome-associated membrane protein. It is characterized by the triad of hypertrophic cardiomyopathy, myopathy, and intellectual disability. Whereas the molecular and pathophysiological mechanisms underlying this disorder have been previously reported and continue to be explored, the cognitive deficits and psychiatric comorbidities manifested in DD remain an understudied topic. We systematically assessed cognitive abilities and psychiatric comorbidities in 13 males and females. Most of the participants in our cohort (n = 9; 75%) had an IQ score within the normal range, while only one participant had intellectual disability. Participants' performance on the Cognitive Neuropsychiatric Battery (CNB) showed only mildly impaired cognitive abilities in most modules, except in the executive functioning test, which was low compared to healthy controls. Of note, 69% of the participants met criteria for at least one psychiatric disorder, mainly mood and anxiety disorders, occurring alone or in combination in the same patient. The results of the present study challenge earlier reports suggesting that mental retardation is a core constituent in DD. Of importance, it underscores the need to refer Danon patients to psychiatric assessment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cognição / Doença de Depósito de Glicogênio Tipo IIb / Proteína 2 de Membrana Associada ao Lisossomo / Deficiência Intelectual Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cognição / Doença de Depósito de Glicogênio Tipo IIb / Proteína 2 de Membrana Associada ao Lisossomo / Deficiência Intelectual Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Israel