Retinal vascular function in asymptomatic individuals with a positive family history of cardiovascular disease
نویسندگان
چکیده
منابع مشابه
Association of Family History With Cardiovascular Disease in Hypertensive Individuals in a Multiethnic Population
BACKGROUND Hypertension alone is a poor predictor of the individual risk of cardiovascular disease. Hereditary factors of which hypertension is merely a marker may explain why some hypertensive individuals appear more susceptible to cardiovascular disease, and why some ethnicities have more often seemingly hypertension-related cardiovascular disease than others. We hypothesize that, in hyperten...
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Acroangiodermatitis (AAD), also known as Pseudo-Kaposi’s sarcoma, is a rare benign angioproliferative disease associated with chronic venous insufficiency (CVI) or other vascular disorders. We present an 81-year-old male with plaque-like cutaneous lesions, which had progressive erythematous margins, severe pain, and intense pruritus, as well as bilateral swollen and painful feet. It was around ...
متن کاملFamily history of cardiovascular disease.
Evidence Where possible, odds ratios (ORs) have been converted to relative risks (RRs). • A total of 2302 male and female Framingham offspring study participants with parental history of premature CVD (father < 55 years, mother < 65 years) were analyzed for CVD risk.1 After 8 years of followup, CVD increased 75% with paternal and about 60% with maternal history of premature CVD. • Using the sam...
متن کاملPrevalence of thrombophilia in asymptomatic individuals with a family history of thrombosis.
OBJECTIVE The present study investigates the prevalence of thrombophilia in individuals with first or/and second degree family history of thromboembolism. MATERIAL-METHODS The study group consisted of 68 individuals with a first or second degree family history of venous or arterial thromboembolism, but without a personal history of thrombosis. The activity of ATIII, PC, PS, FVIII, FΧΙΙ and to...
متن کاملA Case Report of Incontinentia Pigmenti in a Newborn with Positive Family History Extending Over Three Generations
Background: Incontinentia pigmenti (IP), also known as Bloch-Sulzberger syndrome, is a rare X-linked dominant genodermatosis that presents at the time of birth or soon after birth with cutaneous manifestation. This disorder may also affect the ectodermal tissues, such as the central nervous system, skeletal system, eyes, hair, nails, and teeth. The dermatological findings occur in four successi...
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ژورنال
عنوان ژورنال: Acta Ophthalmologica
سال: 2018
ISSN: 1755-375X
DOI: 10.1111/aos.13783