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Stomatologiia (Mosk) ; 98(1): 61-63, 2019.
Artigo em Russo | MEDLINE | ID: mdl-30830095

RESUMO

The paper presents a clinical case of congenital cleft palate as a manifestation of 22q11.2 deletion syndrome accompanied by other systemic disorders having direct impact on functional indicators and perioperative period during cleft surgery. Specific for 22q11.2 deletion syndrome endocrine disorders affect the facial development. Multidisciplinary approach contributes to the early optimal treatment outcome and prevents further postoperative disturbances in maxillofacial development.


Assuntos
Fissura Palatina , Craniossinostoses , Síndrome de DiGeorge , Fissura Palatina/genética , Face , Humanos
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