کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8752296 | 1594450 | 2017 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Swyer syndrome: The gender swayer?
ترجمه فارسی عنوان
ساییدر سایبری: جنس جنسیت
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موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
پزشکی و دندانپزشکی (عمومی)
چکیده انگلیسی
46XY complete gonadal dysgenesis (SWYER SYNDROME) is a rare type of Disorder of Sex Development. Herein we report a 15Â years-old child, reared as female, presented with complaints of primary amenorrhoea, without short stature or Turner's stigmata. Secondary sexual development was normal. Biochemically, luteinizing hormone (LH) was 23.29Â mIU/ml and follicle stimulating hormone (FSH) was 54.94Â mIU/ml. Serum estradiol level was 15.33Â pg/ml (21-51), and Testosterone was 14.04Â ng/dl. USG abdomen revealed a small uterus with thinned endometrium. MRI Abdomen showed hypoplastic uterus with non-visualized B/L ovaries (? Complete/pure gonadal dysgenesis). Patient had withdrawal bleeding with estrogen progesterone challenge test. Karyotype analysis revealed 46XY with no evidence of mosaicism. Based on these results a diagnosis of Swyer Syndrome (complete gonadal dysgenesis: Disorder of Sexual Development) was suspected. Patient was managed with a multidisciplinary approach and various issues were discussed.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Alexandria Journal of Medicine - Volume 53, Issue 2, June 2017, Pages 197-200
Journal: Alexandria Journal of Medicine - Volume 53, Issue 2, June 2017, Pages 197-200
نویسندگان
Jaideep Khare, Prasun Deb, Prachi Srivastava, Babul H. Reddy,