Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record update

GROWing Up With Rare GENEtic Syndromes ….When Children With Complex Genetic Syndromes Reach Adult Age

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Open original source record ↗

Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04463316
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:36.097170+00:00
Published At
2023-09-06T00:00:00+00:00
Record Updated At
2023-09-06
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Prader-Willi Syndrome", "PWS-like Syndrome", "Silver Russel Syndrome", "Congenital Hypopituitarism", "Klinefelter (XXY-)Syndrome", "Congenital Adrenal Hyperplasia", "XXXXY Syndrome", "XXYY Syndrome", "XXXX Syndrome (Tetra-X Syndrome)", "Disorders of Sex Development", "Turner Syndrome", "46, XY DSD", "Tuberous Sclerosis", "Neurofibromatosis", "Albright Hereditaire Osteodystrofie", "Cornelia de Lange Syndrome", "Saethre-Chotzen Syndrome", "17p- Deletiesyndrome", "VCF Syndrome", "POLR3A Mutatie", "Ohdo Syndrome", "Jacobsen Syndrome / 11 q Syndrome", "Myrhe Syndrome", "CHARGE Syndrome", "1q25-32 Deletie", "Bardet Biedl Syndrome", "Rett Syndrome", "22q11 Deletion Syndrome", "Allan-Herndon-Dudley Syndrome", "Kallmann Syndrome", "Rare Bone Disorders", "Noonan Syndrome", "Williams-Beuren Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-09-06"
protocolSection.identificationModule.nctId
"NCT04463316"
protocolSection.identificationModule.officialTitle
"GROWing Up With Rare GENEtic Syndromes \u2026.When Children With Complex Genetic Syndromes Reach Adult Age"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Prader-Willi Syndrome (protocolSection.conditionsModule.conditions)
  • PWS-like Syndrome (protocolSection.conditionsModule.conditions)
  • Silver Russel Syndrome (protocolSection.conditionsModule.conditions)
  • Congenital Hypopituitarism (protocolSection.conditionsModule.conditions)
  • Klinefelter (XXY-)Syndrome (protocolSection.conditionsModule.conditions)
  • Congenital Adrenal Hyperplasia (protocolSection.conditionsModule.conditions)
  • XXXXY Syndrome (protocolSection.conditionsModule.conditions)
  • XXYY Syndrome (protocolSection.conditionsModule.conditions)
  • XXXX Syndrome (Tetra-X Syndrome) (protocolSection.conditionsModule.conditions)
  • Disorders of Sex Development (protocolSection.conditionsModule.conditions)
  • Turner Syndrome (protocolSection.conditionsModule.conditions)
  • 46, XY DSD (protocolSection.conditionsModule.conditions)
  • Tuberous Sclerosis (protocolSection.conditionsModule.conditions)
  • Neurofibromatosis (protocolSection.conditionsModule.conditions)
  • Albright Hereditaire Osteodystrofie (protocolSection.conditionsModule.conditions)
  • Cornelia de Lange Syndrome (protocolSection.conditionsModule.conditions)
  • Saethre-Chotzen Syndrome (protocolSection.conditionsModule.conditions)
  • 17p- Deletiesyndrome (protocolSection.conditionsModule.conditions)
  • VCF Syndrome (protocolSection.conditionsModule.conditions)
  • POLR3A Mutatie (protocolSection.conditionsModule.conditions)
  • Ohdo Syndrome (protocolSection.conditionsModule.conditions)
  • Jacobsen Syndrome / 11 q Syndrome (protocolSection.conditionsModule.conditions)
  • Myrhe Syndrome (protocolSection.conditionsModule.conditions)
  • CHARGE Syndrome (protocolSection.conditionsModule.conditions)
  • 1q25-32 Deletie (protocolSection.conditionsModule.conditions)
  • Bardet Biedl Syndrome (protocolSection.conditionsModule.conditions)
  • Rett Syndrome (protocolSection.conditionsModule.conditions)
  • 22q11 Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • Allan-Herndon-Dudley Syndrome (protocolSection.conditionsModule.conditions)
  • Kallmann Syndrome (protocolSection.conditionsModule.conditions)
  • Rare Bone Disorders (protocolSection.conditionsModule.conditions)
  • Noonan Syndrome (protocolSection.conditionsModule.conditions)
  • Williams-Beuren Syndrome (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.