54 top medical experts on Jansen type metaphyseal chondrodysplasia across 10 countries and 3 U.S. states, including 6 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Jansen type metaphyseal chondrodysplasia: A rare autosomal dominant skeletal dysplasia characterized by short-limbed short stature (due to severe metaphyseal changes that are often discovered in childhood by imaging), waddling gait, bowed legs, contracture deformities of the joints, short hands with clubbed fingers, clinodactyly, prominent upper face and small mandible, as well as chronic parathyroid hormone-independent hypercalcemia, hypercalciuria, and mild hypophosphatemia.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Little People of America, Inc.
617 Broadway #518
Sonoma, CA 95476
Toll-free: 1-888-572-2001
Telephone: +1-714-368-3689
Fax: +1-707-721-1896
E-mail: info@lpaonline.org
Website: https://www.lpaonline.org/
- Little People UK
P.O Box 1292
Peterborough
PE2 2NT
United Kingdom
Telephone: 07925893398
E-mail: info@littlepeopleuk.org
Website: https://littlepeopleuk.org/
- The Jansen’s Foundation
20105 Hopper Street
Elkhorn, NE 68022
Telephone: +1-1-402-457-9886
E-mail: info@thejansensfoundation.org
Website: https://www.thejansensfoundation.org/
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- Synonyms: Jansen Type Metaphyseal Chondrodysplasia, Murk Jansen Type Metaphyseal Chondrodysplasia, Metaphyseal chondrodysplasia Murk Jansen type, Murk Jansen type metaphyseal chondrodysplasia
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