4.2 Article

Unexplained regression in Down syndrome: Management of 51 patients in an international patient database

期刊

AMERICAN JOURNAL OF MEDICAL GENETICS PART A
卷 188, 期 10, 页码 3049-3062

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WILEY
DOI: 10.1002/ajmg.a.62922

关键词

catatonia; Down syndrome; Down syndrome disintegrative disorder; regression; trisomy 21; unexplained regression in down syndrome

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Research on the management of regression in individuals with Down syndrome is limited. This study collected data from seven clinics and found that many patients showed improvement in function over time and that IVIG treatment may be effective. These findings lay the foundation for future research and clinical practice guidelines.
Research to guide clinicians in the management of the devastating regression which can affect adolescents and young adults with Down syndrome is limited. A multi-site, international, longitudinal cohort of individuals with a clinical diagnosis of Unexplained Regression in Down syndrome (URDS) was collated through seven Down syndrome clinics. Tiered medical evaluation, a 28-item core symptom list, and interim management are described naturalistically. Improvement-defined by the percentage of baseline function on a Parent-reported Functional Score, overall improvement in symptoms on a Clinician-administered Functional Assessment, or report of management type being associated with improvement-was analyzed. Improvement rates using ECT, IVIG, and others were compared. Across seven clinics, 51 patients with URDS had regression at age 17.6 years, on average, and showed an average 14.1 out of 28 symptoms. Longitudinal improvement in function was achieved in many patients and the medical management, types of treatment, and their impact on function are described. Management with intravenous immunoglobulin (IVIG) was significantly associated with higher rate of improvement in symptoms at the next visit (p = 0.001). Our longitudinal data demonstrates that URDS is treatable, with various forms of clinical management and has a variable course. The data suggests that IVIG may be an effective treatment in some individuals. Our description of the management approaches used in this cohort lays the groundwork for future research, such as development of standardized objective outcome measure and creation of a clinical practice guideline for URDS.

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