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Case Series: Variable Genetic Expressivity In Crouzon Syndrome- A Comparative Report Of Three Cases

    Authors

    • Dr. Puneeta Vohra 1
    • Dr. Shaik Rabbani 2
    • Dr. Archna Nagpal 3
    • Dr.Vundela Muni Sravani 4
    • Dr. Gaurav Sharma 5
    • Dr. Sourabh Ramesh Joshi 6
    • Dr. Rahul VC Tiwari 7

    1 Associate Professor, Department Of Oral Medicine And Radiology, Faculty Of Dental Sciences, SGT University, Gurgaon, Haryana, India

    2 Post Graduate Student, Department of Oral and Maxillofacial surgery, C.K.S Theja institute of institute of Dental sciences and Research, Tirupati, AP

    3 Professor and HOD, Department of Oral Medicine and Radiology, Faculty Of Dental Sciences, SGT University, Gurgaon, Haryana, India

    4 Post Graduate Student, Department of Oral and Maxillofacial Surgery,C.K.S Theja Institute of Dental Sciences and Research, Tirupathi, AP

    5 Dental Student, Boston University, Massachusetts, United States of America

    6 Reader, Department Of Pediatric Dentistry, Rural Dental College, Pravara Institute Of Medical Sciences, Loni, Taluka Rahata, Ahmednagar, Maharashtra, India

    7 OMFS, FOGS, PhD Scholar, Dept of OMFS, Narsinbhai Patel Dental College and Hospital, Sankalchand Patel University, Visnagar, Gujarat, India.

,

Document Type : Research Article

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Abstract

Despite the intense research, the clinical manifestation of syndromic craniosynostosis patients remains an enigma. Human skull is made up of various bone joints connected by sutures. The sutures fuse in later life after the complete growth ofthe brain. If any of these sutures close early, it may encumber the normal growth of the brain. In craniosynostosis there are disturbances in the growth of the skull which are caused by premature synostosis at one or more cranial sutures, resulting in typical deformities of the vault called as dyscrania. Crouzon syndrome is an emblematic example of craniosynostosis. Cranial malformations in crouzon syndrome depend on the order and rate of progression of sutural synostosis. Thus, physical appearance varies from patient to patient. In this article we intend to compare two patients with crouzon syndrome and a clinically non syndromic patient with beaten metal appearance radiographically. The idea behind this is that each syndromic patient is distinctive and a separate approach for treatment of such patients is desired.

Keywords

  • craniofacial
  • Crouzon
  • Premature
  • synostosis
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European Journal of Molecular & Clinical Medicine
Volume 8, Issue 2
January 2021
Page 12-22
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  • Article View: 397
  • PDF Download: 473

APA

Vohra, D. P., Rabbani, D. S., Nagpal, D. A., Sravani, D. M., Sharma, D. G., Joshi, D. S. R., & Tiwari, D. R. V. (2021). Case Series: Variable Genetic Expressivity In Crouzon Syndrome- A Comparative Report Of Three Cases. European Journal of Molecular & Clinical Medicine, 8(2), 12-22.

MLA

Dr. Puneeta Vohra; Dr. Shaik Rabbani; Dr. Archna Nagpal; Dr.Vundela Muni Sravani; Dr. Gaurav Sharma; Dr. Sourabh Ramesh Joshi; Dr. Rahul VC Tiwari. "Case Series: Variable Genetic Expressivity In Crouzon Syndrome- A Comparative Report Of Three Cases". European Journal of Molecular & Clinical Medicine, 8, 2, 2021, 12-22.

HARVARD

Vohra, D. P., Rabbani, D. S., Nagpal, D. A., Sravani, D. M., Sharma, D. G., Joshi, D. S. R., Tiwari, D. R. V. (2021). 'Case Series: Variable Genetic Expressivity In Crouzon Syndrome- A Comparative Report Of Three Cases', European Journal of Molecular & Clinical Medicine, 8(2), pp. 12-22.

VANCOUVER

Vohra, D. P., Rabbani, D. S., Nagpal, D. A., Sravani, D. M., Sharma, D. G., Joshi, D. S. R., Tiwari, D. R. V. Case Series: Variable Genetic Expressivity In Crouzon Syndrome- A Comparative Report Of Three Cases. European Journal of Molecular & Clinical Medicine, 2021; 8(2): 12-22.

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