The hypertelorism—hypospadias syndrome

Silva, Elias O. da

doi:10.1111/j.1399-0004.1983.tb00433.x

Clinical Genetics

1983

DOI: 10.1111/j.1399-0004.1983.tb00433.x

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The hypertelorism—hypospadias syndrome

Elias O. da Silva

Abstract: An affected family (five cases and one questionable case) with the hypertelorism‐hypospadias syndrome is reported. Inheritance is either autosomal or X‐linked dominant.

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Cited by 11 publications

References 5 publications

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Further delineation of the Opitz G/BBB syndrome: Report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature

et al. 1998

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The combination of complex congenital heart disease (double outlet right ventricle with pulmonary atresia, malalignment ventriculoseptal defect, right-sided aortic arch with left ductus arteriosus) and bladder exstrophy occurred in an infant with Opitz syndrome. Neither of these defects has previously been reported in association with Opitz syndrome. These malformations, which are midline defects, further characterize this syndrome as an impairment in midline development. The spectrum of congenital heart disease and genitourinary anomalies seen in Opitz syndrome is reviewed.

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Further delineation of the Opitz G/BBB syndrome: Report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature

et al. 1998

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Male‐to‐male transmission of the hypertelorism‐hypospadias (BBB) syndrome

Stoll¹,

A²,

Berland³

et al. 1985

Am. J. Med. Genet.

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Ocular hypotelorism, submucosal cleft palate, and hypospadias: A new autosomal dominant syndrome

Schilbach¹,

Rott²,

Neri³

et al. 1988

Am. J. Med. Genet.

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The hypertelorism—hypospadias syndrome

Abstract: An affected family (five cases and one questionable case) with the hypertelorism‐hypospadias syndrome is reported. Inheritance is either autosomal or X‐linked dominant.

Cited by 11 publications

References 5 publications

Further delineation of the Opitz G/BBB syndrome: Report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature

Further delineation of the Opitz G/BBB syndrome: Report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature

Male‐to‐male transmission of the hypertelorism‐hypospadias (BBB) syndrome

Ocular hypotelorism, submucosal cleft palate, and hypospadias: A new autosomal dominant syndrome

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