CHARGE syndrome with both primary and secondary hypogonadism

Bibliographic Details
Title: CHARGE syndrome with both primary and secondary hypogonadism
Authors: Yuki Yoshida, Soichiro Ogawa, Satoru Meguro, Akifumi Onagi, Ryo Tanji, Kanako Matsuoka, Seiji Hoshi, Junya Hata, Yuichi Sato, Hidenori Akaihata, Masao Kataoka, Motohide Uemura, Yoshiyuki Kojima
Source: IJU Case Reports, Vol 7, Iss 3, Pp 197-200 (2024)
Publisher Information: Wiley, 2024.
Publication Year: 2024
Collection: LCC:Diseases of the genitourinary system. Urology
Subject Terms: CHARGE syndrome, hypogonadism, testicular dysgenesis syndrome, Diseases of the genitourinary system. Urology, RC870-923
More Details: Introduction CHARGE syndrome is a rare disorder that causes congenital abnormalities in multiple organs, including secondary hypogonadism. We report, herein, a unique case of CHARGE syndrome with both primary and secondary hypogonadism and discuss the possible causes and pathogenesis in this patient. Case presentation A 15‐year‐old boy with delayed secondary sexual characteristics and non‐palpable testes was referred to our hospital. Physical examination and detection of a chromodomain‐helicase‐deoxyribonucleic acid‐binding protein 7 gene mutation confirmed CHARGE syndrome. Hormone stimulation tests suggested both primary and secondary hypogonadism. Laparoscopic bilateral orchiectomy was performed because of decreased testosterone production and atrophy in both testes. Pathological examination of the testes revealed maturation arrest, germ cell neoplasm in situ, and decreased expression of steroid synthase. Conclusion This appears to be the first report of CHARGE syndrome with both primary and secondary hypogonadism demonstrated in endocrinological and histological examinations.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2577-171X
Relation: https://doaj.org/toc/2577-171X
DOI: 10.1002/iju5.12694
Access URL: https://doaj.org/article/910dbdd6701f4a339c3ec13db7bb7702
Accession Number: edsdoj.910dbdd6701f4a339c3ec13db7bb7702
Database: Directory of Open Access Journals
More Details
ISSN:2577171X
DOI:10.1002/iju5.12694
Published in:IJU Case Reports
Language:English