Clin2
NCT01995305Possibly a fitAvailable

Genetic testing for children with fanconi anemia

Fanconi AnemiaAutosomal or Sex Linked Recessive Genetic DiseaseBone Marrow Hematopoiesis Failure, Multiple Congenital Abnormalities, and Susceptibility to Neoplastic Diseases.Hematopoiesis Maintainance.

Part of Blood & lymphatic, Genetic & congenital, Hormones & metabolism clinical trials.

This study uses advanced genetic testing to look at the DNA of children with Fanconi anemia and their parents. The goal is to learn more about the genetic causes of the condition, which might help guide future care.

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

Phase
N/A
Ages
1 month to 18 years
Study type
Expanded Access

Who can take part

  • Your child must have a confirmed diagnosis of Fanconi anemia.
  • Your child must be treated at the Blood Disease Hospital (likely in China).
  • Your child must be under 18 years old (the study says 'children').
  • You must be able to provide consent for your child to join the study.
  • The study is taking place between August 2010 and July 2011.

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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