Literature DB >> 17686676

[Mixed gonadal dysgenesis associated with an isodicentric Y chromosome].

László Ságodi1, Enikô Sólyom, András Tóth, Anna Kékesi, Erika P Tardy, Eva Borbás, Teofil Rétfalvi, Akos Kiss, Anikó Korcsmáros.   

Abstract

Authors report a case of mixed gonadal dysgenesis with a karyotype containing an isodicentric Y chromosome in mosaic form, which was diagnosed in an infant. They emphasize the necessity of the special investigations of newborn with perineoscrotal hypospadia and bilateral or unilateral maldescent testes immediately after birth. The result of accurate evaluation provides correct sex assignment and the prevention of the neoplastic degeneration of a dysgenetic gonad.

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Year:  2007        PMID: 17686676     DOI: 10.1556/OH.2007.28108

Source DB:  PubMed          Journal:  Orv Hetil        ISSN: 0030-6002            Impact factor:   0.540


  2 in total

1.  Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.

Authors:  Zafer Cetin; Mesut Parlak; Ozden Altiok Clark; Gungor Karaguzel; Guven Luleci; Iffet Bircan; Sibel Berker-Karauzum
Journal:  Eur J Pediatr       Date:  2013-05-08       Impact factor: 3.183

2.  A rare case of mixed gonadal dysgenesis with mosaicism 45, X/46, X, +mar.

Authors:  Fahimeh Soheilipour; Ommolbanin Abed; Babak Behnam; Mohammadreza Abdolhosseini; Peyman Alibeigi; Abdolreza Pazouki
Journal:  Int J Surg Case Rep       Date:  2014-12-12
  2 in total

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