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1.
BMC Med Genet ; 14: 49, 2013 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-23634718

RESUMO

BACKGROUND: Global developmental delay and mental retardation are associated with X-linked disorders including Hunter syndrome (mucopolysaccharidosis type II) and Fragile X syndrome (FXS). Single nucleotide mutations in the iduronate 2-sulfatase (IDS) gene at Xq28 most commonly cause Hunter syndrome while a CGG expansion in the FMR1 gene at Xq27.3 is associated with Fragile X syndrome. Gene deletions of the Xq27-28 region are less frequently found in either condition with rare reports in females. Additionally, an association between Xq27-28 deletions and skewed X-inactivation of the normal X chromosome observed in previous studies suggested a primary role of the Xq27-28 region in X-inactivation. CASE PRESENTATION: We describe the clinical, molecular and biochemical evaluations of a four year-old female patient with global developmental delay and a hemizygous deletion of Xq27.3q28 (144,270,614-154,845,961 bp), a 10.6 Mb region that contains >100 genes including IDS and FMR1. A literature review revealed rare cases with similar deletions that included IDS and FMR1 in females with developmental delay, variable features of Hunter syndrome, and skewed X-inactivation of the normal X chromosome. In contrast, our patient exhibited skewed X-inactivation of the deleted X chromosome and tested negative for Hunter syndrome. CONCLUSIONS: This is a report of a female with a 10.6 Mb Xq27-28 deletion with skewed inactivation of the deleted X chromosome. Contrary to previous reports, our observations do not support a primary role of the Xq27-28 region in X-inactivation. A review of the genes in the deletion region revealed several potential genes that may contribute to the patient's developmental delays, and sequencing of the active X chromosome may provide insight into the etiology of this clinical presentation.


Assuntos
Deleção Cromossômica , Cromossomos Humanos X , Deficiências do Desenvolvimento/genética , Síndrome do Cromossomo X Frágil/genética , Inativação do Cromossomo X , California , Pré-Escolar , Hibridização Genômica Comparativa , Feminino , Proteína do X Frágil da Deficiência Intelectual/genética , Síndrome do Cromossomo X Frágil/diagnóstico , Humanos , Fenótipo
2.
J Am Acad Nurse Pract ; 24(5): 313-23, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22551336

RESUMO

PURPOSE: To evaluate the role of counseling for patients undergoing screening for type 2 herpes simplex virus (HSV-2). Using pre- and post-screening questionnaires, we evaluated correlations between demographic factors, measures of self-efficacy and follow-through with the screening test, and willingness to take antiviral medication and share results with sexual partners. DATA SOURCES: Subjects (N= 115) were recruited as part of usual care at a private, urban family practice. A total of 111 subjects completed pre-screening questionnaires, and 38 completed post-screening questionnaires. CONCLUSIONS: The overwhelming majority of participants were (a) willing to undergo screening; (b) take suppressive antiviral medication if necessary; (c) share their results with sexual partners; and (d) consider safer sexual practices as a consequence of screening. Older patients were less willing to consider daily antiviral medication. Men who have sex with men (MSM) had lower perceived susceptibility to HSV-2 but were more likely to undergo and report screening. IMPLICATIONS FOR PRACTICE: Future research should include predictive models for determining the most appropriate patients to screen for HSV-2 and best practices for those who test positive. Shared decision making between patients and advanced practice nurses regarding the risks and benefits of screening for HSV-2 should be a component visits that include sexually transmitted disease screening. Particular attention should be paid to those at higher risk for contracting the virus, including patients with HIV and MSM.


Assuntos
Aconselhamento Diretivo/métodos , Infecções por Herpesviridae/diagnóstico , Herpesvirus Humano 2 , Autoeficácia , Adulto , Feminino , Pesquisas sobre Atenção à Saúde , Conhecimentos, Atitudes e Prática em Saúde , Infecções por Herpesviridae/epidemiologia , Infecções por Herpesviridae/psicologia , Homossexualidade Masculina , Humanos , Masculino , Programas de Rastreamento/métodos , Pessoa de Meia-Idade , Satisfação do Paciente , Projetos Piloto , Atenção Primária à Saúde , Assunção de Riscos , São Francisco/epidemiologia , Estatísticas não Paramétricas , Adulto Jovem
3.
J Adolesc Health ; 35(6): 505-8, 2004 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15581531

RESUMO

The seroprevalence and determinants of hepatitis C virus (HCV) infection among adolescents in juvenile detention centers in Riverside County was assessed. Among 728 participants, 16 (2.2%, 95% CI 1.1%, 3.3%) demonstrated serologic evidence of HCV infection. Adolescents with a history of injection drug use (adjusted OR = 10.8, 95% CI 2.6, 45.3, P < .001) were more likely to be HCV seropositive, however the frequency of reported injection drug use was just 4%, and only 12% of HCV infection could be attributable to injecting drugs in this population. Additional information is needed on risk factors for HCV infection in adolescent populations. The relatively low level of HCV infection observed in this juvenile detention population underscores the opportunity for implementation of targeted intervention efforts.


Assuntos
Comportamento do Adolescente , Hepatite C/diagnóstico , Hepatite C/epidemiologia , Delinquência Juvenil/estatística & dados numéricos , Abuso de Substâncias por Via Intravenosa/epidemiologia , Abuso de Substâncias por Via Intravenosa/virologia , Adolescente , Comportamento do Adolescente/psicologia , California/epidemiologia , Distribuição de Qui-Quadrado , Intervalos de Confiança , Feminino , Humanos , Masculino , Uso Comum de Agulhas e Seringas/estatística & dados numéricos , Razão de Chances , Psicologia do Adolescente , Fatores de Risco , Estudos Soroepidemiológicos
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