Abstract
Hallermann-Streiff syndrome was independently described by Hallermann in 1948 and Streiff in 1950. The syndrome is characterized by proportionate short stature and craniofacial dysostoses consisting of skeletal, ophthalmologic, and cutaneous defects.
References
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Chen, H. (2017). Hallermann-Streiff Syndrome. In: Atlas of Genetic Diagnosis and Counseling. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2401-1_112
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DOI: https://doi.org/10.1007/978-1-4939-2401-1_112
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