Gardner-silengo-wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy

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Abstract

Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome is a disorder of male (46,XY) gonadal dysgenesis, thought to be either an X-linked recessive or an autosomal recessive disorder. The propositus in our report presented with multiple congenital anomalies including micrognathia, cleft palate, congenital heart defect with D-transposition, double outlet right ventricle, PFO, VSD, PDA and pulmonary valve stenosis and gonadal dysgenesis. Chromosome analysis showed a 46, XY, t(1;7)(q32,q22.1) der(10) t(3;10) (q21;q26)pat karyotype. This represents a rare case of autosomal aneuploidy associated with Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome and suggests genetic heterogeneity for this syndrome. Partial monosomy of 10q also shares many of the prominent features of genito-palato-cardiac syndrome, including gonadal dysgenesis, cardiac defects and facial features. Monosomy for distal 10q may present as a phenocopy of Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome. Alternatively, unmasking of a recessive allele on distal 10q may result in genito-palato-cardiac syndrome, thus potentially localizing a candidate region for the gene to 10q26→ qter. © 2009 Wiley-Liss, Inc.

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APA

Golabi, M., James, A. W., Desai, N., Culver, K., & Cotter, P. D. (2009). Gardner-silengo-wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy. American Journal of Medical Genetics, Part A, 149(4), 693–697. https://doi.org/10.1002/ajmg.a.32755

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