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Importance: The functional limitations and long-term dependence of children with congenital Zika syndrome (CZS) may lead to changes in maternal occupational roles, which can have a negative impact on mothers' well-being and mental health.Objective: To investigate changes in occupational roles and their effects on the mental health of mothers who have a child with CZS.

Introduction: The family lives sociocultural transformations requesting more of the man in the children's daily cares with deficiency because commonly the mothers wrap up in the tasks causing an overload in the daily tasks. Objective: To verify the paternal participation in the daily care to the child with microcephaly, to trace the paternal socio-demographic profile, to know the main activities performed by the fathers and to analyze their perception in the participation of the children daily cares. Method: This is a quantitative and qualitative study, held in 3 Specialized Centers in Rehabilitation in the city of Maceio, AL, Brazil, with 23 fathers of children with microcephaly, in the period of September of 2017 to February of 2018. For the quantitative component, a specific questionnaire and analysis through descriptive statistics, arithmetic average and percentage were used. In the qualitative component, a semi-structured interview was used that was analyzed through the Analysis of Content.Results: Most of the fathers live with the child, 70% make available 2 hours of time for the son's daily care, and there was a larger paternal engagement in the activities of playing on 74% and social participation on 91%. In the qualitative component, 4 parents participated in the interview, and three thematic categories emerged: Paternal perception and self-assessment regarding the participation in the daily care of the child with microcephaly; Factors associated with paternal engagement in the daily care; and Identification of the activities performed by the fathers in the care to the child with microcephaly. Conclusion: The fathers engaged in daily care to assist the mothers and not as the protagonist. It stands out the need for strategies that favor such participation in the dimensions of the care to the child with a disability.

A Doença de Huntington (DH) é uma desordem neurodegenerativa de herança autossômica dominante. Os sintomas se caracterizam por uma tríade, distúrbio dos movimentos, mudanças de humor e comprometimento cognitivo. Trata-se de um estudo transversal, descritivo, com objetivo de identificar o estado funcional dos pacientes com DH, a partir de uma amostra censitária, analisando todos os pacientes diagnosticados no município. A pesquisa foi realizada em um município alagoano, com vinte indivíduos diagnosticados com a doença. Para alcançar os objetivos, foi utilizado um questionário validado para a população brasileira, a Medida de Independência Funcional (MIF), o qual identifica a dependência de uma pessoa referente a sua capacidade funcional, avaliando a dificuldade nas realizações de tarefas do autocuidado, mobilidade e comunicação. A partir da análise dos resultados foi possível identificar as relações de parentesco existentes, o tipo de assistência médica e de reabilitação que cada participante está submetido e a sua condição funcional, levando os pesquisadores a caracterizar cada um deles e concluir que a limitação no acesso a serviços especializados em reabilitação física e a ausência de aconselhamento genético leva à continuidade dos casos e à alta prevalência dessa patologia no município.