Marfan syndrome, a rare hereditary connective tissue disorder caused by mutations in fibrillin-1, can affect many organ systems, especially the cardiovascular system. Previous research has paid less attention to health-related quality of life and prospective studies on this topic are needed. The aim...
§based on analysis of Taiwan National Health Insurance database from 2000 to 2012 §2,329 patients (58% men) had Marfan syndrome §overall prevalence 10.2 per 100,000 persons §peak prevalence 32.3 per 100,000 persons aged 15-19 years ...
NHS VIDEOS | Mental health: Big White Wall Big White Wall is an online mental health network where people can anonymously be open about what is on their mind. This video is aimed at members of the a... N Choices - Department of Health 被引量: 0发表: 0年 NHS VIDEOS | Lung cancer ...
Marfan syndrome is a multisystem connective tissue disorder usually associated with mutation in fibrillin, and occasionally with mutation in TGFBR1 or 2. The clinical diagnosis is made using the Ghent nosology, which will unequivocally diagnose or exclude Marfan syndrome in 86% of cases. Use of a...
Dural ectasia is common in people with Marfan syndrome and most frequently occurs in the lower portions of the spine. It may cause headache, lower back pain, or other neurologic problems such as bowel or bladder weakness. Utambuzi wa Ugonjwa wa Marfan A doctor's evaluati...
What 7 Feet Tall Isaiah Austin Having Marfan Syndrome Suggest To Professional Basketball Players So I was not able to write much in the last 2 weeks due to a combination of issues: legal, technical, and health related. Hopefully most of those issues have been resolved. ...
Mild intrinsic cardiomyopathy in patients with Marfan syndrome (MFS) has consistently been evidenced by independent research groups. So far, little is known about the long-term evolution and pathophysiology of this finding. To gain more insights into the
Marfan Syndrome - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - Medical Consumer Version.
§based on analysis of Taiwan National Health Insurance database from 2000 to 2012 §2,329 patients (58% men) had Marfan syndrome §overall prevalence 10.2 per 100,000 persons §peak prevalence 32.3 per 100,000 persons aged 15-19 years ...
FBN1 mutation screening can also be indicated in an affected patient with reproductive issues. A prenatal test for Marfan syndrome is rarely requested, but it is expected that the greater availability of mutation testing of the FBN1 gene will increase requests for prenatal diagnosis. Prenatal ...