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Diagnosis and evaluation of Crouzon syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2009; 19 (5): 318-320
in English | IMEMR | ID: emr-91669
ABSTRACT
Crouzon syndrome is an autosomal dominant condition characterized by craniosynostosis with associated dentofacial anomalies. This report describes the different clinical features in two affected individuals of different families with particularn reference to characteristic findings of this syndrome
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Index: IMEMR (Eastern Mediterranean) Main subject: Orbit / Cranial Sutures / Craniosynostoses / Mutation Type of study: Case report Limits: Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2009

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Index: IMEMR (Eastern Mediterranean) Main subject: Orbit / Cranial Sutures / Craniosynostoses / Mutation Type of study: Case report Limits: Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2009