Literature DB >> 16042329

True hermaphroditism with characteristics of Klinefelter's syndrome: a rare presentation.

Pinar Isguven1, Metin Yildiz, Ilknur Arslanoglu, Erdal Adal, Muferret Erguven, Sitki Tuzlali.   

Abstract

True hermaphroditism, a very rare cause of intersex, is usually diagnosed during the newborn period in the course of evaluating ambiguous genitalia. As an exception we report an unusual case of a 14.5 year-old boy with phenotypically near-normal male genitalia and bilaterally descended gonads, who was seen for evaluation of gynecomastia and hematuria. His eunuchoid body habitus and mild mental retardation were compatible with Klinefelter's syndrome. He had a low level of free testosterone (15.2 pmol/l), and high level of estradiol (264.3 pmol/l) for his age. The patient was diagnosed as true hermaphroditism with 46,XX /47,XXY karyotype causing an ovotestis with inguinal uterus hernia in the left scrotum and a dysgenetic testis in the right scrotum.

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Year:  2005        PMID: 16042329     DOI: 10.1515/jpem.2005.18.6.603

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  5 in total

1.  Klinefelter Syndrome Mosaicism 46,XX/47,XXY: A New Case and Literature Review.

Authors:  Chayada Tangshewinsirikul; Wirada Dulyaphat; Thipwimol Tim-Aroon; Rachanee Parinayok; Takol Chareonsirisuthigul; Veerawat Korkiatsakul; Jariya Waisayarat; Pokket Sirisreetreerux; Yada Tingthanatikul; Duangrurdee Wattanasirichaigoon
Journal:  J Pediatr Genet       Date:  2020-06-17

2.  Ovotestis in Adolescence: 2 Case Reports.

Authors:  Jyoti D Chouhan; David I Chu; Antoinette Birs; Louise C Pyle; Jason P Van Batavia; Rebecca L Linn; Susan J Back; Pierre Russo; Kassa Darge; Thomas F Kolon; Arun K Srinivasan
Journal:  Urology       Date:  2017-04-13       Impact factor: 2.649

Review 3.  An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature.

Authors:  Tinka Hovnik; Eva Zitnik; Magdalena Avbelj Stefanija; Sara Bertok; Katarina Sedej; Vesna Bancic Silva; Tadej Battelino; Urh Groselj
Journal:  Genes (Basel)       Date:  2022-04-23       Impact factor: 4.141

4.  A rare case of lateral ovotesticular disorder with Klinefelter syndrome mosaicism 46, XX/47, XXY: An unusual presentation.

Authors:  Shyam M Talreja; Indraneel Banerjee; Sher Singh Yadav; Vinay Tomar
Journal:  Urol Ann       Date:  2015 Oct-Dec

5.  A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome.

Authors:  Noor Shafina Mohd Nor; Muhammad Yazid Jalaludin
Journal:  Int J Pediatr Endocrinol       Date:  2016-06-02
  5 in total

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