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Get the free CRANE: Cleft Registry and Audit Network England, Wales

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CRANE Database ExportsCRANE Database T: 020 7869 6610 E: crane@rcseng.ac.uk W: www.cranedatabase.org.ukCRANE Database Exports. Prepared by the CRANE Database Project Team The CRANE Database system
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01
Obtain an application form for the crane cleft registry.
02
Fill out all the required personal information such as name, address, contact details.
03
Provide detailed information about the cleft condition, including date of diagnosis, type of cleft (e.g. lip, palate), and any previous treatments.
04
Submit any medical records, imaging reports, or test results related to the cleft condition.
05
Review the filled out form for accuracy and ensure all necessary information is included.
06
Submit the completed form to the designated registry office or organization.

Who needs crane cleft registry and?

01
Individuals born with a cleft lip or palate
02
Parents or guardians of children born with a cleft lip or palate
03
Healthcare professionals involved in the treatment and care of patients with cleft lip or palate
04
Researchers and institutions studying cleft lip and palate conditions
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Crane cleft registry is a database where individuals can register and report cases of crane cleft defects.
Healthcare providers, hospitals, and clinics are required to file crane cleft registry.
To fill out crane cleft registry, healthcare providers need to provide detailed information on the patient, diagnosis, and treatment.
The purpose of crane cleft registry is to track and monitor cases of crane cleft defects for research and statistical purposes.
Information such as patient demographics, diagnosis details, treatment received, and outcome must be reported on crane cleft registry.
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