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Journal of Orthopedic Education 8(1):p 23-25, January-April 2022. | DOI: http://dx.doi.org/10.21088/joe.2454.7956.8122.3
Case Report
A Case Report Apert Syndrome
Santhosh Kumar M , Supraja P1 , Santhosh Kumar M2 , Anitha C3
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Journal of Orthopedic Education 8(1):p 23-25, January-April 2022. | DOI: http://dx.doi.org/10.21088/joe.2454.7956.8122.3
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| Supraja P, Santhosh Kumar M, Anitha C / A Case Report Apert Syndrome / J Orth. Edu. 2022;8(1):23–25. |
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Abstract
Apert syndrome (acrocephalosyndactyly) is an autosomal dominant disorder characterized by craniosynostosis, syndactyly, and midfacial malformation.
Keywords: Possible mechanism of injury and operative procedures are discussed.
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| Supraja P, Santhosh Kumar M, Anitha C / A Case Report Apert Syndrome / J Orth. Edu. 2022;8(1):23–25. |
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DOI: http://dx.doi.org/10.21088/joe.2454.7956.8122.3
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