Due to this complexity, determining genetic and downstream biological influences on sexual dimorphism in humans is challenging. Sex chromosome aneuploidies, such as Turner syndrome (X0) and Klinefelter syndrome (XXY), are common genetic conditions in humans. The study of individuals with sex ...
Acute Respiratory Failure and Acute Respiratory Distress Syndrome in ACS Patient: What Are the Indications for Acute Intervention?An understanding of respiratory failure and acute respiratory distress syndrome (ARDS) is paramount to the knowledge base of an emergency general surgeon as their trauma and ...
Acute coronary syndrome (ACS):Blood flow is sometimes suddenly reduced to your heart. Because that can lead to a heart attack,ACSis treated like an emergency. If you have severe chest pain, seek help right away. Atherosclerotic coronary artery disease:Over time, a sticky, fatty substance called...
Acute coronary syndrome (ACS):Blood flow is sometimes suddenly reduced to your heart. Because that can lead to a heart attack,ACSis treated like an emergency. If you have severe chest pain, seek help right away. Atherosclerotic coronary artery disease:Over time, a sticky, fatty substance called...
Patients with complex rare genetic syndromes (CRGS) have combined medical problems affecting multiple organ systems. Pediatric multidisciplinary (MD) care has improved life expectancy, however, transfer to internal medicine is hindered by the lack of ade
night eating syndrome and purging disorder, and avoidant-restrictive food intake disorder [10]. Mainly anorexia nervosa, bulimia nervosa, and binge eating disorders are characterised by disturbed eating behaviour associated with concerns about weight and shape or by disinterest in food, phobic avoidance...
AAKSISAmerican Association for Klinefelter Syndrome Information and Support(Chicago, IL) Copyright 1988-2018AcronymFinder.com, All rights reserved. Suggest new definition Want to thank TFD for its existence?Tell a friend about us, add a link to this page, or visitthe webmaster's page for free ...
Mutations in the human NDUFS4 gene can lead to complex I deficiency and Leigh-like syndrome, a human inborn neurological disorder [77]. There are at least three mutations linked to this syndrome that are affecting S173-NDUFS4. One mutation consists of a 5 base pair duplication, which disru...
IntroductionThe evidence for beta-blocker use in patients after acute coronary syndrome (ACS), particularly in those with left ventricular (LV) dysfunction, dates from the late 1990s. We aimed to assess the role of beta-blockers in a contemporary population of patients with ACS....
The XPC group is the most common in the United States and Europe and is found in 43% of XP patients [11,12]. Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis-Cacchione Syndrome and a Novel XPC Mutation Xia et al., "XPC gene polymorphisms and risk of idiopathic azoospe...