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Oklahoma Medical Research Foundation | OMRF

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Home - OMRF News - Archives for spondyloepiphyseal dysplasia

spondyloepiphyseal dysplasia

The Mystery of Madison

Could OMRF provide the answers Melissa Cain so desperately sought about her daughter’s illness?

Oklahoma teen lives with unique skeletal disorder

December 3, 2019

Sydney Rutz is one in five billion.

Filed Under: News Tagged With: bone, condition, disease, disorder, Gaffney, genetic, growth, Lijun, mary, mbtps1, middle school, mutation, news, newsok, OKC, Oklahoma Medical Research Foundation, OMRF, patient, patrick, rutz, scientist-news, scoliosis, skeletal, skeleton, spondyloepiphyseal dysplasia, sydney, Xia, yukon

1 In 5 Billion

There are people who suffer from rare diseases. And then there’s Sydney Rutz, who has a genetic condition never before identified–until a group of OMRF scientists took on her case.

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OKLAHOMA MEDICAL RESEARCH FOUNDATION
825 NE 13th St.
Oklahoma City, OK 73104
(405) 271-6673
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