Asunto(s)
Población Negra , Economía , Memoria , Identificación Social , Estrés Psicológico , Violencia , Población Negra/educación , Población Negra/etnología , Población Negra/historia , Población Negra/legislación & jurisprudencia , Población Negra/psicología , Economía/historia , Economía/legislación & jurisprudencia , Historia del Siglo XVIII , Historia del Siglo XIX , Humanos , Madagascar/etnología , Estrés Psicológico/economía , Estrés Psicológico/etnología , Estrés Psicológico/historia , Violencia/economía , Violencia/etnología , Violencia/historia , Violencia/legislación & jurisprudencia , Violencia/psicologíaRESUMEN
1. Diplopia may require a simple change in the patient's glasses, various types of surgical correction, or even treatment for a life-threatening condition. Your job is to determine the urgent nature of the problem and have the patient scheduled in your office, clinic, or hospital appropriately. 2. When questions of diplopia arise, establish whether the diplopia is still present when either the right or left eye is covered (monocular or binocular diplopia). 3. Monocular diplopia is most always optical in nature. Binocular diplopia is caused by either aniseikonia (a difference in the relative sizes of the retinal images perceived by the patient) or, more commonly, misalignment of the visual axes.
Asunto(s)
Diplopía/diagnóstico , Diagnóstico Diferencial , Diplopía/etiología , Diplopía/enfermería , Humanos , Evaluación en EnfermeríaRESUMEN
Among early life SLE mice, the male F1 hybrids of NZW X BXSB crosses are unique by their much earlier onset of glomerulonephritis (GN) (evident by 2 1/2 months of age), progressive hypertension, and high frequency of degenerative cardiovascular disease (CVD) with myocardial infarcts. In contrast, their female counterparts and the other kinds of SLE mice have later onset of GN, minimal hypertension, and lower incidence of CVD. The etiopathogenesis of these F1 males' disease was investigated by reciprocally transferring syngeneic lymphoid cells into lethally irradiated F1 male and female mice. As a result, female recipients of male lymphoid cells developed accelerated GN, hypertension, and severe CVD, but the male recipients of female lymphoid cells (at comparable ages) had delayed SLE, remained normotensive, and were spared coronary or myocardial damage. These findings strongly indicate that the hypertension and CVD of these F1 males originate from immunologic abnormalities rather than from other nonlymphoid factors.