Clin2
NCT07497477Possibly a fitNot yet recruiting

Methylation patterns in growth disorders

Imprinting DisorderMLIDMulti-locus Imprinting DisturbanceDifferentially Methylated RegionsMolecular Diagnosis

Part of Genetic & congenital clinical trials.

This study compares the methylation patterns (chemical tags on DNA that control gene activity) in people with certain growth disorders (like Beckwith-Wiedemann syndrome, Silver-Russell syndrome, or Temple syndrome) to those with other genetic conditions. It aims to improve diagnosis for these rare conditions.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
96 people
Ages
6 months to 70 years
Study type
Interventional

Who can take part

  • You have had genetic testing for a growth disorder, and either your methylation results are normal (as a control) or you have a confirmed diagnosis of Beckwith-Wiedemann syndrome, Silver-Russell syndrome, or Temple syndrome.
  • You are covered by a health insurance plan (like social security) or are a beneficiary; AME is not accepted.
  • You or your parents/guardians can sign a consent form.
  • You are not under any legal restriction that prevents you from receiving study information.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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