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Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report

Year 2012, Volume: 3 Issue: 1, 23 - 27, 01.06.2012

Abstract

Background: The aim of this study is to evaluate a man-like patient of 68-year-old who was referred to our department with history of hermaphroditism. Case: A 65 years old patient was referred to Dicle University Medical Faculty Department of Medical Biology for karyotype analysis. On systemic, gynecologic and ultrasound examination of the patient was detected 150 cm height, 55 kg weight, female phenotype, female type breasts and hair, approximately 3,5 cm clitoris, normal labium major, fused labium minor, 0.5x1.0 cm opening and 9 cm depth of vagina, 60x37x30 cm size of uterus and 20x15 mm each ovaries. The patient had menstruated regularly during reproductive period from menarche to menopause. The karyotype of patient was performed in peripheric blood sample. The chromosomal constitution of the patient whose Barr Body was positive, was found to be 46,XX. Molecular PCR (polymerase chain reaction) technique for detection of SRY (specific region of Y chromosome) sequences is used to determine whether the SRY gene is present in the patient. The SRY gene in this case was negative. Conclusion: In spite offemale karyotype and phenotype the patient lived as a male until 65 years. This case has ignored due to social and economic conditions, therefore we think that the patient can be considered for publication

References

  • de la Chapelle A, Hortling H, Niemi M, Wennstroem J.XX sex chromosomes in a human male.First case.Acta Med Scand, 175(Suppl 412):25–28, 1964 de la Chapelle A.Theetiology of maleness in XX men. Hum Genetics, 58:105–116, 1981.
  • Rajender S, Rajani V, Gupta N.J.et al. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility.Molecular Human Reproduction, 12(5): 341-346,2006 www.bookrags.com/research/xx-male-syndrome-wog/
  • Vilain E.J.46,XX TesticularDisorder of Sex Development, Gene Reviews,Bookshelf ID: NBK1416, Last Updite 2009
  • Berkovitz GD. Abnormalities of gonaddeterminationanddifferentiation. Sem Perinatology. 16: 289-298, 1992
  • Vorona E, Zitzmann M, Gromoll Jet al.Clinical, endocrinologicandepigeneticfeatures of the 46, XX malesyndromecomparedto 47,XXYKlinefelterpatients.TheJournal of ClinicalEndocrinology&Metabolism, 92(9):3458 – , 2007
  • Lang M, Sinn HP, Heilmann P et al.Femalepseudohermaphroditism in congenitaladrenogenitalsyndrome as an incidentalintraoperativefinding in a 68 yearoldpatient. DtschMedWochenschr. 2000 May 26;125(21):660-4.
Year 2012, Volume: 3 Issue: 1, 23 - 27, 01.06.2012

Abstract

References

  • de la Chapelle A, Hortling H, Niemi M, Wennstroem J.XX sex chromosomes in a human male.First case.Acta Med Scand, 175(Suppl 412):25–28, 1964 de la Chapelle A.Theetiology of maleness in XX men. Hum Genetics, 58:105–116, 1981.
  • Rajender S, Rajani V, Gupta N.J.et al. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility.Molecular Human Reproduction, 12(5): 341-346,2006 www.bookrags.com/research/xx-male-syndrome-wog/
  • Vilain E.J.46,XX TesticularDisorder of Sex Development, Gene Reviews,Bookshelf ID: NBK1416, Last Updite 2009
  • Berkovitz GD. Abnormalities of gonaddeterminationanddifferentiation. Sem Perinatology. 16: 289-298, 1992
  • Vorona E, Zitzmann M, Gromoll Jet al.Clinical, endocrinologicandepigeneticfeatures of the 46, XX malesyndromecomparedto 47,XXYKlinefelterpatients.TheJournal of ClinicalEndocrinology&Metabolism, 92(9):3458 – , 2007
  • Lang M, Sinn HP, Heilmann P et al.Femalepseudohermaphroditism in congenitaladrenogenitalsyndrome as an incidentalintraoperativefinding in a 68 yearoldpatient. DtschMedWochenschr. 2000 May 26;125(21):660-4.
There are 6 citations in total.

Details

Other ID JA34ZF22NT
Journal Section Case Report
Authors

Selda Sımsek This is me

Aysegul Turkyılmaz This is me

Hilmi Isı This is me

Diclehan Oral This is me

Selahaddin Tekes This is me

Ahmet Yalınkaya This is me

Publication Date June 1, 2012
Published in Issue Year 2012 Volume: 3 Issue: 1

Cite

APA Sımsek, S., Turkyılmaz, A., Isı, H., Oral, D., et al. (2012). Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report. International Archives of Medical Research, 3(1), 23-27.
AMA Sımsek S, Turkyılmaz A, Isı H, Oral D, Tekes S, Yalınkaya A. Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report. IAMR. June 2012;3(1):23-27.
Chicago Sımsek, Selda, Aysegul Turkyılmaz, Hilmi Isı, Diclehan Oral, Selahaddin Tekes, and Ahmet Yalınkaya. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research 3, no. 1 (June 2012): 23-27.
EndNote Sımsek S, Turkyılmaz A, Isı H, Oral D, Tekes S, Yalınkaya A (June 1, 2012) Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report. International Archives of Medical Research 3 1 23–27.
IEEE S. Sımsek, A. Turkyılmaz, H. Isı, D. Oral, S. Tekes, and A. Yalınkaya, “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”, IAMR, vol. 3, no. 1, pp. 23–27, 2012.
ISNAD Sımsek, Selda et al. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research 3/1 (June 2012), 23-27.
JAMA Sımsek S, Turkyılmaz A, Isı H, Oral D, Tekes S, Yalınkaya A. Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report. IAMR. 2012;3:23–27.
MLA Sımsek, Selda et al. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research, vol. 3, no. 1, 2012, pp. 23-27.
Vancouver Sımsek S, Turkyılmaz A, Isı H, Oral D, Tekes S, Yalınkaya A. Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report. IAMR. 2012;3(1):23-7.

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