Academic Journal
Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report
| العنوان: | Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report |
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| المؤلفون: | Pradyumna Pan |
| المصدر: | International Journal of Pediatrics, Vol 6, Iss 10, Pp 8381-8384 (2018) |
| بيانات النشر: | Mashhad University of Medical Sciences |
| سنة النشر: | 2018 |
| المجموعة: | Directory of Open Access Journals: DOAJ Articles |
| مصطلحات موضوعية: | Child, Genitals, Malformations, Klinefelter syndrome, Pediatrics, RJ1-570 |
| الوصف: | Klinefelter syndrome is characterised by advancing testicular function deterioration causing aspermatogenesis and androgen deficiency. Klinefelter patients characteristically have complete male sex differentiation, and genital anomalies are infrequently associated. Penoscrotal malformations at birth are very rare in this syndrome. Nonetheless, it is important to know the association, as one of the causes of abnormal genitalia at birth. Understanding of the indications of karyotyping can help early detection of these cases. We report a boy who had Klinefelter syndrome with penoscrotal transposition (PST), hypospadias and inguinal hernia. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 2345-5047 2345-5055 |
| Relation: | http://ijp.mums.ac.ir/article_10982_67722cd01399fe35f1f3eabf2ed9f8f0.pdf; https://doaj.org/toc/2345-5047; https://doaj.org/toc/2345-5055; https://doaj.org/article/93661fb3aac24ee69144c219f927f773 |
| DOI: | 10.22038/ijp.2018.32430.2857 |
| الاتاحة: | https://doi.org/10.22038/ijp.2018.32430.2857 https://doaj.org/article/93661fb3aac24ee69144c219f927f773 |
| رقم الانضمام: | edsbas.1954C5A1 |
| قاعدة البيانات: | BASE |
| تدمد: | 23455047 23455055 |
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| DOI: | 10.22038/ijp.2018.32430.2857 |