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GROWing Up With Rare GENEtic Syndromes

Study acronym: GROW UR GENES
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Re-verified, no change to tracked fieldsv2
  2. Minor Study First Submitted
Introduction Rare complex syndromes Patients with complex genetic syndromes, by definition, have combined medical problems affecting multiple organ systems, and intellectual disability is often part of the syndrome. During childhood, patients with rare genetic syndromes receive multidisciplinary and specialized medical care; they usually receive medical care from 3-4 medical specialists. Increased life expectancy Although many genetic syndromes used to cause premature death, improvement of medical care has improved life expectancy. More and more patients are now reaching adult age, and the complexity of the syndrome persists into adulthood. However, until recently, multidisciplinary care was not available for adults with rare genetic syndromes. Ideally, active and well-coordinated health management is provided to prevent, detect, and treat comorbidities that are part of the syndrome. However, after transition from pediatric to adult medical care, patients and their parents often report fragmented poor quality care instead of adequate and integrated health management. Therefore, pediatricians express the urgent need for adequate, multidisciplinary adult follow up of their pediatric patients with rare genetic syndromes. Medical guidelines for adults not exist and the literature on health problems in these adults is scarce. Although there is a clear explanation for the absence of adult guidelines (i.e. the fact that in the past patients with rare genetic syndromes often died before reaching adult age), there is an urgent need for an overview of medical issues at adult age, for 'best practice' and, if possible, for medical guidelines. The aim of this study is to get an overview of medical needs of adults with rare genetic syndromes, including: 1. comorbidities 2. medical and their impact on quality of life 3. medication use 4. the need for adaption of medication dose according to each syndrome Methods and Results This is a retrospective file study. Analysis will be performed using SPSS version 23 and R version 3.6.0.
Trial Details
NCT Number NCT04463316
Lead Sponsor dr. Laura C. G. de Graaff-Herder
Conditions
(from sponsor)
Prader-Willi Syndrome, PWS-like Syndrome, Silver Russel Syndrome, Congenital Hypopituitarism, Klinefelter (XXY-)Syndrome, Congenital Adrenal Hyperplasia, XXXXY Syndrome, XXYY Syndrome +25 more
Related terms 22q11 Deletion Syndrome, Acrocephalosyndactylia, Adrenal Hyperplasia, Congenital, Allan-Herndon-Dudley syndrome, Bardet-Biedl Syndrome, Blepharophimosis syndrome Ohdo type, CHARGE Syndrome, De Lange Syndrome, DiGeorge Syndrome, Disorder of Sex Development, 46,XY, Disorders of Sex Development, Jacobsen Distal 11q Deletion Syndrome, Kallmann Syndrome, Klinefelter Syndrome, Neurofibromatoses, Noonan Syndrome, Prader-Willi Syndrome, Rett Syndrome, Tetrasomy X, Tuberous Sclerosis, Turner Syndrome, Williams Syndrome
Enrollment 600 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov