LA56 Pierre Robin syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2022-02


Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. This condition is referred to as a sequence because the posterior cleft palate is a secondary defect associated with abnormal mandibular development: mandibular hypoplasia occurring early in gestation causes the tongue to be maintained high-up in the oral cavity, preventing fusion of the palatal shelves.

synonyms

free demo
request yours today
newsletter
free subscription
pricing
for any budget

Thank you for choosing Find-A-Code, please Sign In to remove ads.