Literature DB >> 1844355

Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype.

L R Meacham1, K J Winn, F L Culler, J S Parks.   

Abstract

We have studied two unrelated genetic males with a novel constellation of genital, cardiac, and pulmonary malformations. The genital abnormalities consisted of a true double vagina, retention of Müllerian structures, and undervirilization of the external genitalia. Both infants had complex cyanotic congenital heart defects, hypoplastic right lungs, anomalous pulmonary venous return, and abnormalities of the diaphragm. One patient had rhabdomyomatous dysplasia of the lungs. The cause of this malformation pattern is unknown. There was no family history of similar defects, no consanguinity, no known exposure to teratogens, and no chromosome abnormality. The retention of Müllerian structures and undervirilization of male genitalia in these cases could be the result of failure in production of adequate amounts of testosterone and Müllerian inhibitory factor at appropriate times in gestation. Because the developing human vagina is at no stage a duplicate structure, a double vagina cannot be the result of arrested genital differentiation. The unusual occurrence of a true double vagina should lead to careful pulmonary and cardiac evaluation.

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Year:  1991        PMID: 1844355     DOI: 10.1002/ajmg.1320410420

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

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2.  Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.

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3.  Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.

Authors:  Patrick Y Jay; Malgorzata Bielinska; Jonathan M Erlich; Susanna Mannisto; William T Pu; Markku Heikinheimo; David B Wilson
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Review 4.  46,XY disorders of sex development and congenital diaphragmatic hernia: a case with dysmorphic facies, truncus arteriosus, bifid thymus, gut malrotation, rhizomelia, and adactyly.

Authors:  Edward D Esplin; Hassan Chaib; Michael Haney; Brock Martin; Margaret Homeyer; Alexander E Urban; Jonathan A Bernstein
Journal:  Am J Med Genet A       Date:  2015-04-21       Impact factor: 2.802

5.  Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.

Authors:  Yo Han Ahn; Eu Jin Park; Hee Gyung Kang; Seong Heon Kim; Hee Yeon Cho; Jae Il Shin; Joo Hoon Lee; Young Seo Park; Kyo Sun Kim; Il-Soo Ha; Hae Il Cheong
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Review 6.  Molecular genetics of congenital diaphragmatic defects.

Authors:  Malgorzata Bielinska; Patrick Y Jay; Jonathan M Erlich; Susanna Mannisto; Zsolt Urban; Markku Heikinheimo; David B Wilson
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  6 in total

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