سندرم Cornelia de Lange و معرفي يك مورد شيرخوار مبتلا

Cornelia De Lange Syndrome and Representation Of an Infant Patient

Cornelia De Lange is a rare congenital syndrome with multiple anomalies including; Facial dysmorphism, hirsutism, height, weight and head circumflex retardations, cardiac defects, gastrointestinal and renal defects and extremity anomaly. Prevalence of this syndrome is 1 to 30000 or 1 to 50000. The diagnosis of this syndrome is based on clinical evidence. Genetic foundation is known to have two forms including dominant autosomal and is X linked. Often mutations are NIPBL and SMC 1L1. The aim of this paper is to show a case of Cornelia De Lange syndrome.