Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences

OBJECTIVE: the purpose of this paper is to report the first case of megaurethra in a fetus with Meckel syndrome and in a fetus with femal pseudoermaphroditism

Bibliographische Detailangaben
Veröffentlicht in:Journal of prenatal medicine. - 2007. - 8(2014), 3-4 vom: 10. Apr., Seite 42-6
1. Verfasser: Di Meglio, Letizia (VerfasserIn)
Weitere Verfasser: Mazzarelli, Laura Letizia, Boscaino, Amedeo, Cancemi, Dino, Morelli, Franco, Lonardo, Maria Concetta, Lonardo, Valeria, Friso, Patrizia, Spampanato, Carmine, Urciuoli, Maria, Ventruto, Marialuisa, Ventruto, Valerio
Format: Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Journal of prenatal medicine
Schlagworte:Case Reports Meckel syndrome congenital megaurethra female pseudoermaphroditism prenatal diagnosis
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245 1 0 |a Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences 
264 1 |c 2014 
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500 |a Date Completed 12.08.2015 
500 |a Date Revised 29.09.2020 
500 |a published: Print 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a OBJECTIVE: the purpose of this paper is to report the first case of megaurethra in a fetus with Meckel syndrome and in a fetus with femal pseudoermaphroditism 
520 |a RESULTS: the former case refers to a fetus of 13 weeks gestation with the three following prominent anomalies, observed by transonic scan and confirmed by autopsy: congenital megaurethra, anal atresia, single umbelical artery. The latter case refers to a fetus of 18 weeks gestation. Autopsy confirmed penile malformation and revealed ovaries in the abdomen. The karyotype was 46,XX with normal molecular karytype. The megaurethra was discovered by sonography at 18 weeks gestation. Autopsy confirmed penile malformation and revealed ovaries in the abdomen. The karyotype was 46,XX with normal molecular karyotype (Array-CGH, 1 Mb of resolution) 
520 |a METHODS: transonic scan, autopsy, karyotype, array-CGH 
520 |a CONCLUSIONS: the first prenatal cases of two genetic syndromes with megaurethra have been reported, concening respectively a fetus with Meckel syndrome and a fetus with femal pseudoermaphroditism. The latter was confirmed by both autopsy and the normal female 46,XX karyotype 
650 4 |a Case Reports 
650 4 |a Meckel syndrome 
650 4 |a congenital megaurethra 
650 4 |a female pseudoermaphroditism 
650 4 |a prenatal diagnosis 
700 1 |a Mazzarelli, Laura Letizia  |e verfasserin  |4 aut 
700 1 |a Boscaino, Amedeo  |e verfasserin  |4 aut 
700 1 |a Cancemi, Dino  |e verfasserin  |4 aut 
700 1 |a Morelli, Franco  |e verfasserin  |4 aut 
700 1 |a Lonardo, Maria Concetta  |e verfasserin  |4 aut 
700 1 |a Lonardo, Valeria  |e verfasserin  |4 aut 
700 1 |a Friso, Patrizia  |e verfasserin  |4 aut 
700 1 |a Spampanato, Carmine  |e verfasserin  |4 aut 
700 1 |a Urciuoli, Maria  |e verfasserin  |4 aut 
700 1 |a Ventruto, Marialuisa  |e verfasserin  |4 aut 
700 1 |a Ventruto, Valerio  |e verfasserin  |4 aut 
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