Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report

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Pan Pradyumna

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Journal Paper

Paper Information

Journal: Journal of Pediatric Perspectives Year:2018 | Volume:6 | Issue:10 (58) Page(s): 8381-8384

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Information Journal Paper

Title

Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report

Author(s)

Pan Pradyumna | Issue Writer Certificate

Keywords

Child

Genitals

Malformations

Klinefelter syndrome

Abstract

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.

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APA: Copy

Pan, Pradyumna. (2018). Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report. INTERNATIONAL JOURNAL OF PEDIATRICS, 6(10 (58)), 8381-8384. SID. https://sid.ir/paper/337603/en

Vancouver: Copy

Pan Pradyumna. Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report. INTERNATIONAL JOURNAL OF PEDIATRICS[Internet]. 2018;6(10 (58)):8381-8384. Available from: https://sid.ir/paper/337603/en

IEEE: Copy

Pradyumna Pan, “Prepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report,” INTERNATIONAL JOURNAL OF PEDIATRICS, vol. 6, no. 10 (58), pp. 8381–8384, 2018, [Online]. Available: https://sid.ir/paper/337603/en

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