Email this article Setre-Chotzen syndrome in an 8-year-old girl
- Authors: Kotov V.L.1, Meyerson E.M.1, Il'ina V.K.1, Bruskina V.Y.1
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Affiliations:
- Central Institute of Traumatology and Orthopedics named after N.N. Priorov
- Issue: Vol 6, No 2 (1999)
- Pages: 71-72
- Section: From Practical Experience
- URL: https://journals.rcsi.science/0869-8678/article/view/104842
- DOI: https://doi.org/10.17816/vto104842
- ID: 104842
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Abstract
Acrocephalosyndactyly (type III), or Saethre-Chotzen syndrome, according to the International Nomenclature of Hereditary Skeletal Diseases, belongs to the group of dysostoses, manifested by deformities of individual bones or their combinations, and is included in the subgroup of dysostoses with a primary lesion of the face and skull. The type of inheritance is autosomal dominant.
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##article.viewOnOriginalSite##About the authors
V. L. Kotov
Central Institute of Traumatology and Orthopedics named after N.N. Priorov
Author for correspondence.
Email: info@eco-vector.com
Russian Federation, Moscow
E. M. Meyerson
Central Institute of Traumatology and Orthopedics named after N.N. Priorov
Email: info@eco-vector.com
Russian Federation, Moscow
V. K. Il'ina
Central Institute of Traumatology and Orthopedics named after N.N. Priorov
Email: info@eco-vector.com
Russian Federation, Moscow
V. Y. Bruskina
Central Institute of Traumatology and Orthopedics named after N.N. Priorov
Email: info@eco-vector.com
Russian Federation, Moscow
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