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ACTA2 - actin alpha 2, smooth muscle. Synonym (s): ACTSA. Previous symbol (s) and name (s): actin, alpha 2, smooth muscle, aorta. Type: gene with protein product. Chromosomal location: 10q23.31. OMIM: 102620.
10 Μαρ 2015 · Individuals with ACTA2 mutations present with both type A and type B aortic dissections at significantly younger ages than individuals enrolled in the International Registry of Acute Aortic Dissection (IRAD) study 22 and are likely to report a family history of thoracic aortic disease.
More than 30 ACTA2 gene mutations have been identified in people with familial thoracic aortic aneurysm and dissection (familial TAAD). This disorder involves problems with the aorta, which is the large blood vessel that distributes blood from the heart to the rest of the body.
ICD 10 code for Attention-deficit hyperactivity disorder, combined type. Get free rules, notes, crosswalks, synonyms, history for ICD-10 code F90.2.
ADHD is found in the ICD-10 under the code F90.0.13 Consistent clinical guidelines are important for providing better quality care, evidence-based medical practice and cost-efficient services and for improving clinical outcomes, care planning, multidisciplinary communications and resource allocation.
The findings provide support for a common effect of genes coding for cell adhesion/pathfinding ... nor did they indicate whether such mutations also cause ADHD in adults. A first systematic analysis ... Fasmer OB, Haavik J. Bipolar disorder risk alleles in adult ADHD patients. Genes Brain Behav. 2011;10:418–423. doi: 10.1111/j.1601-183X.2011. ...
16 Αυγ 2018 · The 21st century has witnessed the discovery of multiple rare and common gene variants associated with attention deficit hyperactivity disorder (ADHD), and these discoveries have already provided a starting point for the investigation of the biology of the disorder and novel treatments.
