CHARGE syndrome
Autozomálně dominantní · About 1 in 10,000 births.
A condition caused by variants in CHD7 that typically includes coloboma of the eye, heart defects, choanal atresia, growth and developmental delay, genital differences and ear anomalies with hearing loss.
Co se diagnózou změní
Diagnosis guides hearing, heart, growth and puberty (hormone) assessment.
Analyzované geny
Známé také jako
CHARGE association; coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies; coloboma, heart defects, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear anomalies association; coloboma, heart malformation, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear malformations (CHARGE) association; coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome; Hall-Hittner syndrome
Zahrnuje 1 příbuzný podtyp ↓Skrýt podtypy ↑
- CHD7-related CHARGE syndrome
