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Journal of Pediatrics Review، جلد ۱۰، شماره ۱، صفحات ۷-۷
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چکیده فارسی مقاله
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عنوان انگلیسی Identification of a Novel Mutation in an Iranian Family with 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency; A case series
چکیده انگلیسی مقاله Background: To present the clinical and genetic features of a male ambiguity due to 17beta-hydroxysteroid dehydrogenase 3 (17B-HSD3) deficiency. Case presentation: The proposita was an 11-year-old girl and the first child of a consanguineous family. The external genitalia were completely female and had a short vaginal pouch. She had palpable gonads in her inguinal area and underwent bilateral gonadectomy at the age of two. At age 10, she was referred to our clinic for more evaluation. In pelvic sonography, uterine and ovarian were not seen. Her karyotype was 46, XY and her LH and FSH levels were elevated, and three of the patient's aunts and one of the mother's aunts had similar signs. Conclusion: We identified a novel homozygous missense variation (c.731T>A, p. Ile244Lys) in HSD17B3 gene. This alteration changes Isoleucine to Lysine in exon 10.
کلیدواژه‌های انگلیسی مقاله 17-β-HSD3, Virilization, 46, XY, Iran
نویسندگان مقاله | Abolfazl Heidari
Reference Laboratory of Qazvin Medical University, Qazvin, Iran Sana Medical Genetics Laboratory, Qazvin, Iran.


| Ali Homaei
Student of Medicine, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.


| Fatemeh Saffari
Associate Professor of Pediatric Endocrinology, Children Growth Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.
نشانی اینترنتی http://jpr.mazums.ac.ir/browse.php?a_code=A-10-960-2&slc_lang=en&sid=1
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کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده Endocrinology
نوع مقاله منتشر شده Case Report and Review of Literature
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