Family caregiving involves the provision of care by family members and self-care by patients, with the two groups participating together in illness-related care. A convenience sample of 100 patients and 100 unrelated family caregivers were surveyed to examine their perceptions of the caregiving skills they perform, the difficulty they experience in performing certain skills, and their associated learning needs. Descriptive analysis of data revealed differences in the type of activities patients and caregivers perform, the perceived difficulty of caregiving tasks, and their need for assistance. Uncertainty about disease stage poses important implications for educators.
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http://dx.doi.org/10.1007/s13187-010-0076-z | DOI Listing |
JACC Adv
December 2024
Department of Medicine, The Cardiac Clinic, University of Cape Town and Groote Schuur Hospital, Cape Town, South Africa.
Background: Cardiomyopathies are an important cause of heart failure in Africa yet there are limited data on etiology and clinical phenotypes.
Objectives: The IMHOTEP (African Cardiomyopathy and Myocarditis Registry Program) was designed to systematically collect data on individuals diagnosed with cardiomyopathy living in Africa.
Methods: In this multicenter pilot study, patients (age ≥13 years) were eligible for inclusion if they had a diagnosis of cardiomyopathy or myocarditis.
Nest sharing by birds, or the phenomenon where multiple individuals of different species contribute genetically and parentally to offspring in a single nest, is a rare form of cooperative breeding that has only occasionally been reported in socially monogamous birds. Here we describe, both behaviorally and genetically, the unique case of two female birds, a western kingbird () and a western kingbird × scissor-tailed flycatcher () hybrid, simultaneously occupying (and likely co-incubating eggs in) a single nest. Both females provisioned nestlings, and they did this in two consecutive years (producing four fledglings each year).
View Article and Find Full Text PDFGenome Med
January 2025
Otology & Neurotology Group CTS495, Instituto de Investigación Biosanitario, Ibs.GRANADA, Universidad de Granada, 18071, Granada, Spain.
Background: Familial Meniere's disease (FMD) is a rare polygenic disorder of the inner ear. Mutations in the connexin gene family, which encodes gap junction proteins, can also cause hearing loss, but their role in FMD is largely unknown.
Methods: We retrieved exome sequencing data from 94 individuals in 70 Meniere's disease (MD) families.
J Psychiatr Res
December 2024
Centre for Wellbeing, Resilience and Recovery, Neuroscience Research Australia, Sydney, NSW, Australia; School of Psychology, University of New South Wales, Sydney, NSW, Australia; The Black Dog Institute, Sydney, NSW, Australia. Electronic address:
Early life stress (ELS) significantly influences mental health in later stages of life. Yet it is unclear whether recent life events lessen or intensify the effects of ELS on present wellbeing and distress. We addressed this question in 1064 healthy community adults with a normative range of wellbeing and distress.
View Article and Find Full Text PDFAm J Med Genet A
January 2025
Medical Genetics and Genomic Medicine-Department of Translational Medicine, School of Medical Sciences, Campinas, Brazil.
Myhre syndrome is a rare disorder caused by pathogenic gain-of-function variants in the SMAD4 gene. Most of the patients have had de novo variants. There are several instances of autosomal dominant inheritance, and penetrance appears to be complete.
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