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MENUVolume : VIII, Issue : III, March - 2019
A CLASSICAL CASE OF CROUZON SYNDROME
Dr. G. Priyanka, Dr A. Vasundhara
Abstract :
The Crouzon syndrome or craniofacial dysostosis is a rare disease that affects the craniofacial skeleton development. Although it is uncommon, it has a transmission risk of 50% when one of the parents is a carrier. One third of cases arise sporadically through fresh mutations.
Keywords :
Crouzon Syndrome Craniosynostosis Craniofacial dysostosis Turricephaly Fibroblast growth factor gene (FGFR)
Article:
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DOI : 10.36106/ijsr
Cite This Article:
A CLASSICAL CASE OF CROUZON SYNDROME, DR. G. PRIYANKA, DR A. VASUNDHARA INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-8 | Issue-3 | March-2019
Number of Downloads : 111
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A CLASSICAL CASE OF CROUZON SYNDROME, DR. G. PRIYANKA, DR A. VASUNDHARA INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-8 | Issue-3 | March-2019
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