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World Cancer Day 2024: Expert Shares Steps That May Help Prevent Breast Cancer

Instead of focusing on how to treat breast cancer, the focus should be placed on preventing it, and thus breast cancer will become more than treatable but preventable in the future.

The Hidden Risk of Thyroid Cancer in Young Women: Prevention and Early Detection Recommendations

The Hidden Risk of Thyroid Cancer in Young Women: Prevention and Early Detection Recommendations
archyde.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from archyde.com Daily Mail and Mail on Sunday newspapers.

EEOC Sanctions Employer For GINA Violations Relating To Collection Of Employees' Family Members' COVID Test Results - Employee Rights/ Labour Relations

Know your family medical history: your health could depend on it

If a blood relative suffered from a genetic condition or chronic disease, tell your doctor – they will know what to test you for and the signs you need to check for.

Frontiers | A Novel Probable Pathogenic PSEN2 Mutation p.Phe369Ser Associated With Early-Onset Alzheimer's Disease in a Chinese Han Family: A Case Report

Department of Neurology, The First Affiliated Hospital of Anhui Medical University, Hefei, China The pathogenesis of Alzheimer s disease is complex, and early-onset Alzheimer s disease (EOAD) is mostly influenced by genetic factors. Presenilin-1, presenilin-2 (PSEN2), and amyloid precursor protein are currently known as the three main causative genes for autosomal dominant EOAD, with the PSEN2 mutation being the rarest. In this study, we reported a 56-year-old Chinese Han proband who presented with prominent progressive amnesia, aphasia, executive function impairment, and depression 5 years ago. The 3-year follow-up showed that the patient experienced progressive brain atrophy displayed on magnetic resonance imaging (MRI) and dramatic cognitive decline assessed by neuropsychological evaluation. This patient was clinically diagnosed as EOAD based on established criteria. A heterozygous variant (NM 000447.2: c.1106T>C) of PSEN2 was identified for the first time in this patient and her

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