Congenital stenosis of vena cava inferior superior. We performed all analyses in Stata version Congenital malformations, deformations and chromosomal abnormalities Note Codes from this chapter are not for use on maternal or fetal records. Absence of larynx Agenesis of larynx Atresia of larynx Congenital cleft thyroid cartilage Congenital fissure of epiglottis Congenital stenosis of larynx NEC Posterior cleft of cricoid cartilage Q The diagnosis of fibrous dysplasia can often be made based on the clinical and radiographic appearance, but in some cases may be confirmed with a tissue biopsy.
Other specified congenital deformities of feet Includes: Findings from this study suggest codes that might be most efficient for surveillance and research on CFM Table 4. The colored squares show from where the results are found. Musculoskeletal deformities of skull face and jaw. Absence of fallopian tube and broad ligament Accessory fallopian tube and broad ligament Atresia of fallopian tube and broad ligament Congenital malformation of fallopian tube or broad ligament NOS.
Q CONGENITAL FACIAL ASYMMETRY
Even if a specific code for CFM were to be proposed immediately, it would not be implemented for at least several years. Specifically, the queries identified any patient seen at either hospital who had received one or more of the CFM codes. We classified individuals as having a CFM diagnosis case or not non-case based on whether individuals met the eligibility criteria. Birth defects can vary from mild to severe. Congenital malformation of vulva NOS.
Congenital diverticulum of esophagus Includes: Bicuspid aortic valve Congenital aortic insufficiency. Because we did not perform physical examinations, it is possible that some CFM patients were misclassified as non-cases. Apert syndrome Cleidocranial dysostosis Craniosynostosis Craniosynostosis repair Craniosynostosis repair - discharge Head and face reconstruction Pierre Robin syndrome Skull x-ray Treacher-Collins syndrome. With the use of a specific CFM code, these areas of inquiry could be explored through hospital discharge databases, national healthcare databases, and birth defects surveillance programs. Early congenital syphilitic oculopathy.