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Chromosome 10q Deletion Syndrome

What is Chromosome 10q Deletion Syndrome?

 

An description of Chromosome 10q Deletion Syndrome has not been added yet.
Acknowledgement of Chromosome 10q Deletion Syndrome has not been added yet.
Prevalence Information of Chromosome 10q Deletion Syndrome has not been added yet.
Synonyms for Chromosome 10q Deletion Syndrome has not been added yet.
Cause of Chromosome 10q Deletion Syndrome has not been added yet.
Symptoms for Chromosome 10q Deletion Syndrome has not been added yet.
Diagnosis of Chromosome 10q Deletion Syndrome has not been added yet.
Diagnostic tests of Chromosome 10q Deletion Syndrome has not been added yet
Treatments of Chromosome 10q Deletion Syndrome has not been added yet.
Prognosis of Chromosome 10q Deletion Syndrome has not been added yet.
Tips or Suggestions of Chromosome 10q Deletion Syndrome has not been added yet.
References of Chromosome 10q Deletion Syndrome has not been added yet.
Welcome & Please Write Created by QueegQueeg
Last updated 24 Jan 2012, 02:48 AM

Posted by QueegQueeg
24 Jan 2012, 02:48 AM

Hello, I am a therapist working with a 4-year-old girl in Philadelphia, PA, USA, who has this deletion -- 10 q 21 of 12 Mb, or 10 q 21.1q 22.1. Her moderate hearing loss and moderate vision loss are being addressed now, and her Physical Therapy and I think Occupational Therapy is happening. She had been viewed as having autistic characteristics, but she has been making such great progress -- attending preschool, having a structured predictable setting, and hearing and seeing better with her hearing aids and glasses -- that I question the view that she is on the (autism) spectrum, but time may tell. If you have any experience with this deletion, please write on this discussion forum. I would be very interested in learning from you. If you have *any experience with any chromosomal deletion* and can offer a family some printed or spoken resources *in MANDARIN*, that would be very much appreciated. Thank you!!! Su (QueegQueeg)

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Cords registry

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access.

Enrolling is easy.

  1. Complete the screening form.
  2. Review the informed consent.
  3. Answer the permission and data sharing questions.

After these steps, the enrollment process is complete. All other questions are voluntary. However, these questions are important to patients and their families to create awareness as well as to researchers to study rare diseases. This is why we ask our participants to update their information annually or anytime changes to their information occur.

Researchers can contact CoRDS to determine if the registry contains participants with the rare disease they are researching. If the researcher determines there is a sufficient number of participants or data on the rare disease of interest within the registry, the researcher can apply for access. Upon approval from the CoRDS Scientific Advisory Board, CoRDS staff will reach out to participants on behalf of the researcher. It is then up to the participant to determine if they would like to join the study.

Visit sanfordresearch.org/CoRDS to enroll.

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I am a mother of 11 year old girl with 10q deletion.i also have twin boys.one of my boys has congenital heart defect that needs lifelong monitoring.Overall,I thanks God for all my kids
I here to try and get support for my niece. Her name is Gaby. She has deletion of 10q25 or 10q26 chromosome. I know its rare, but my sister (Gaby's mother) is in need of emotional support from...
I am a Teacher of the Deaf, working with a preschool girl who has Chromosome 10q deletion, in Philadelphia PA.

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Welcome & Please Write

Created by QueegQueeg | Last updated 24 Jan 2012, 02:48 AM


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