释义 |
CHARGE complex An autosomal dominant disorder typically caused by mutations in the chromodomain helicase DNA-binding protein-7 (CHD7) gene Diagnosis At least 4 major features or 3 major features plus at least 3 minor features Major features Ocular coloboma or microphthalmia, choanal atresia or stenosis, cranial nerve abnormalities, and characteristic auditory and/or auricular anomalies Minor features Distinctive facial dysmorphology, facial clefting, tracheoesophageal fistula, congenital heart defects, genitourinary anomalies, developmental delay, and short stature CHARGE acronym: Coloboma, Heart defects (conotruncal or septal), Atresia of nasal choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies and/or deafnessCHARGE complex A disease of probable neural crest origin, diagnosed when infants have 4 of the acronym's 6 components: Coloboma, Heart defects–conotruncal or septal, Atresia of nasal choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies and/or deafness; other findings: facial palsy, renal anomalies, cleft lip/palateCHARGE com·plex (chahrj kom'pleks) A complex diagnosed in infants with four of the seven components of the CHARGE acronym: coloboma, heart defects, atresia of the nasal choanae, retarded growth and development, genital hypoplasia, ear anomalies, and/or deafness. |