CHARGE syndrome was initially defined as a non-random association of anomalies (Coloboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies/deafness). In 1998, an expert group defined the major (the classical 4C\u27s: Choanal atresia, Coloboma, Characteristic ears and Cranial nerve anomalies) and minor criteria of CHARGE syndrome. Individuals with all four major characteristics or three major and three minor characteristics are highly likely to have CHARGE syndrome. However, there have been individuals genetically identified with CHARGE syndrome without the classical choanal atresia and coloboma. The reported incidence of CHARGE syndrome ranges from 0.1-1.2/10,000 and depends on professional r...
CHARGE syndrome is a well-established multiple-malformation syndrome with distinctive consensus diag...
CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical ...
Background: CHARGE syndrome is an autosomal dominant congenital and rare genetic disease.The prevale...
Abstract CHARGE syndrome was initially defined as a non-random association of anomalies (Coloboma, H...
The CHARGE syndrome is a multiple congenital malformation syndrome occurring in 6-7 per 100,000 live...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
CHARGE (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth and/or dev...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
CHARGE syndrome is a common cause of congenital anomalies. Its rate of incidence is about 1:10,000. ...
BACKGROUND: CHARGE syndrome is a non-random clustering of congenital anomalies including coloboma, h...
CHARGE syndrome is an autosomal dominant disorder characterized by features represented in its acron...
We report on a patient with CHARGE syndrome, as manifested by a coloboma of the optic nerve head, co...
CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical ...
Background/aim: CHARGE syndrome is a rare autosomal dominant disease with multiple congenital anomal...
CHARGE syndrome is a well-established multiple-malformation syndrome with distinctive consensus diag...
CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical ...
Background: CHARGE syndrome is an autosomal dominant congenital and rare genetic disease.The prevale...
Abstract CHARGE syndrome was initially defined as a non-random association of anomalies (Coloboma, H...
The CHARGE syndrome is a multiple congenital malformation syndrome occurring in 6-7 per 100,000 live...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
CHARGE (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth and/or dev...
Background CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the ...
CHARGE syndrome is a common cause of congenital anomalies. Its rate of incidence is about 1:10,000. ...
BACKGROUND: CHARGE syndrome is a non-random clustering of congenital anomalies including coloboma, h...
CHARGE syndrome is an autosomal dominant disorder characterized by features represented in its acron...
We report on a patient with CHARGE syndrome, as manifested by a coloboma of the optic nerve head, co...
CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical ...
Background/aim: CHARGE syndrome is a rare autosomal dominant disease with multiple congenital anomal...
CHARGE syndrome is a well-established multiple-malformation syndrome with distinctive consensus diag...
CHARGE syndrome has been estimated to occur in 1:10,000 births worldwide and shows various clinical ...
Background: CHARGE syndrome is an autosomal dominant congenital and rare genetic disease.The prevale...