BibTex RIS Kaynak Göster

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

Yıl 2012, Cilt: 3 Sayı: 1, 23 - 27, 01.06.2012

Öz

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

Kaynakça

  • 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.
Yıl 2012, Cilt: 3 Sayı: 1, 23 - 27, 01.06.2012

Öz

Kaynakça

  • 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.
Toplam 6 adet kaynakça vardır.

Ayrıntılar

Diğer ID JA34ZF22NT
Bölüm Case Report
Yazarlar

Selda Sımsek Bu kişi benim

Aysegul Turkyılmaz Bu kişi benim

Hilmi Isı Bu kişi benim

Diclehan Oral Bu kişi benim

Selahaddin Tekes Bu kişi benim

Ahmet Yalınkaya Bu kişi benim

Yayımlanma Tarihi 1 Haziran 2012
Yayımlandığı Sayı Yıl 2012 Cilt: 3 Sayı: 1

Kaynak Göster

APA Sımsek, S., Turkyılmaz, A., Isı, H., Oral, D., vd. (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. Haziran 2012;3(1):23-27.
Chicago Sımsek, Selda, Aysegul Turkyılmaz, Hilmi Isı, Diclehan Oral, Selahaddin Tekes, ve Ahmet Yalınkaya. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research 3, sy. 1 (Haziran 2012): 23-27.
EndNote Sımsek S, Turkyılmaz A, Isı H, Oral D, Tekes S, Yalınkaya A (01 Haziran 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, ve A. Yalınkaya, “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”, IAMR, c. 3, sy. 1, ss. 23–27, 2012.
ISNAD Sımsek, Selda vd. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research 3/1 (Haziran 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 vd. “Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report”. International Archives of Medical Research, c. 3, sy. 1, 2012, ss. 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.

All articles published by DUJE are licensed under the Creative Commons Attribution 4.0 International License. This permits anyone to copy, redistribute, remix, transmit and adapt the work provided the original work and source is appropriately cited. 24456