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Oculodentodigital Syndrome

What is Oculodentodigital Syndrome ?

Oculodentodigital Syndrome is a rare genetic disorder resulting in small eyes, underdeveloped teeth, and malformation of the fourth and fifth fingers.

 

 

 

Oculodentodigital Syndrome is a rare genetic disorder resulting in small eyes, underdeveloped teeth, and malformation of the fourth and fifth fingers.

 

 

Acknowledgement of Oculodentodigital Syndrome has not been added yet.
Prevalence Information of Oculodentodigital Syndrome has not been added yet.
Synonyms for Oculodentodigital Syndrome has not been added yet.
Cause of Oculodentodigital Syndrome has not been added yet.
Symptoms for Oculodentodigital Syndrome has not been added yet.
Diagnosis of Oculodentodigital Syndrome has not been added yet.
Diagnostic tests of Oculodentodigital Syndrome has not been added yet
Treatments of Oculodentodigital Syndrome has not been added yet.
Prognosis of Oculodentodigital Syndrome has not been added yet.
Tips or Suggestions of Oculodentodigital Syndrome has not been added yet.
References of Oculodentodigital Syndrome has not been added yet.
Just Joining Created by joessister
Last updated 12 Feb 2010, 08:28 PM

Posted by joessister
12 Feb 2010, 08:28 PM

My brother has ODD Syndrome, and I'm looking to find out if there's new information out there, or others that we can compare notes with. This syndrome has affected my brother since he was very young, with varying issues from epilepsy to gloucoma (he's blind now) to neurological and bone/spine problems. We would love to find out anything new, or others who have this syndrome.

ODDD Created by davidsmeltzer
Last updated 11 Dec 2008, 06:47 PM

Posted by davidsmeltzer
11 Dec 2008, 06:47 PM

I'm hoping others with ODDD might read this community group and come in contact with each other. I'm a 55 year old man who has a definite diagnosis of ODDD. I suffer from weakness in my lower extremities, neurogenic bladder and bowel problems. I'm ansous to compare notes with others with ODDD. I'm also participating in a study of the ODDD and conession 47 that is being done in Canada. I hope someone else will join this community.

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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 have a brother with oculodentaldigital syndrome and looking for any type of support he can get. He's got epilepsy, he's blind, has neurological issues as well as a host of other ailments. His...
I am a 55 year old man who suffrs with the neurological symptoms of the Occulodentodigitaldyslplasia syndrome, a very rare gentic disease that involved demylination and a defect in connexion 47.

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Just Joining

Created by joessister | Last updated 12 Feb 2010, 08:28 PM

ODDD

Created by davidsmeltzer | Last updated 11 Dec 2008, 06:47 PM


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