Disorder of Written Expression
Disorder of written expression is a type of learning disability in which a person’s writing ability falls substantially below normally expected range based on the individual’s age, educational background, and measured intelligence.
Cluster Number:
Wiki Number: W064
Diagnosis: Disorder of Written Expression
US Patients:
World Patients :
Sex Ratio:
Age Onset:
Brain Area:
Symptoms: writing disability where it falls substantially below normal expected range
Progression:
Causes: may also have dyslexia, dyscalculia (math difficulties) or behavior difficulties as learning difficulties
Medications:
Therapies: must support the child or adult positively to reduce fears of shame at previously-poor performances
Youtube Video: Disorder of Written Expression:
Living with Learning Disabilities
Amazon or Library Book: Handwriting Brain-Body Disconnect
Amazon or Library Book:
How to Write a Paragraph
Click the book to link or buy from Amazon.
Click the book to link or buy from Amazon.
4 CURRENT ARTICLES
FROM PUBMED
The world-wide medical research
reports chosen for each diagnosis
Clicking each title opens the
PubMed article’s summary-abstract.
- Suberosin attenuates rheumatoid arthritis by repolarizing macrophages and inhibiting synovitis via the JAK/STAT signaling pathwayby Huan Liu on January 22, 2025
CONCLUSION: SBR significantly reduced clinical symptoms, joint pathological damage, and expression inflammatory cytokine expression in CIA mice. SBR exhibited anti-arthritic effects via the JAK1/STAT3 and JAK1/STAT6 signaling pathways, inhibiting synovial tissue inflammation and M1 macrophage polarization while promoting M2 macrophage polarization. Therefore, SBR may be an effective candidate for RA treatment.
- Assessment of diabetes-specific eating disorder risk in adult patients with diabetesby Afruz Babayeva on January 22, 2025
CONCLUSION: In our study, 35% of patients with diabetes were found to have a risk of DEB, with the risk being higher in the T2D group. Our results emphasize the importance of increasing awareness among physicians and patients about DEB, which is prevalent among patients with diabetes. Early detection of individuals at risk for DEB should be considered a crucial aspect of treatment.
- Zebrafish modeling of atypical PML-RARA isoform from acute promyelocytic leukemia patient and its implications for clinical treatmentby Yin Ye on January 21, 2025
Acute promyelocytic leukemia (APL) is driven by the specific fusion gene PML-RARA produced by chromosomal translocation. Three classic isoforms, L, V, and S, are found in more than 95% of APL patients. However, atypical PML-RARA isoforms are usually associated with uncertain disease progression and treatment prognosis. Recently, we found a novel PML-RARA isoform (named PA) in a patient with atypical clinical characteristics of APL. In order to provide valuable insights for clinical treatment, we...
- The SERPINB4 gene mutation identified in twin patients with Crohn's disease impaires the intestinal epithelial cell functionsby Xiao-Mei Ouyang on January 21, 2025
Crohn's disease (CD) is a chronic inflammatory autoimmune disease of unknown etiology. To identify new targets related to the initiation of CD, we screened a pair of twins with CD, which is a rare phenomenon in the Chinese population, for genetic susceptibility factors. Whole-exome sequencing (WES) of these patients revealed a mutation in their SERPINB4 gene. Therefore, we studied a wider clinical cohort of patients with CD or ulcerous colitis (UC), healthy individuals, and those with a family...