Clinical Pediatric Endocrinology

Clinical Pediatric Endocrinology

Current Issue Vol. 33, No. 1, 2024

Review

GH therapy in children with juvenile idiopathic arthritis: a four-decade review
Giulia Sassano, Saverio La Bella, Armando Di Ludovico, Luciana Breda, Francesco Chiarelli
Clin Pediatr Endocrinol. 2024; 33(1): 1–11.

Case Reports

A Japanese school urine screening program led to the diagnosis of KCNJ11-MODY: A case report
Akito Hattori, Koji Okuhara, Yasuhiro Shimizu, Tohru Ohta, Shigeru Suzuki
Clin Pediatr Endocrinol. 2024; 33(1): 12–16.

A novel variant of IGSF1 in siblings with congenital central hypothyroidism whose diagnosis was prompted by school health checkups
Yoshiko Yamamura, Maki Fukami, Misayo Matsuyama, Hirotake Sawada
Clin Pediatr Endocrinol. 2024; 33(1): 17–22.

A thyroid adenoma in a pubertal male with thyroxine-binding globulin deficiency
Heeyung Kim, Yasuhiro Naiki, Megumi Iwahashi-Odano, Satoshi Narumi, Koichi Ito, Akira Ishiguro
Clin Pediatr Endocrinol. 2024; 33(1): 23–26.

Switching to burosumab from conventional therapy in siblings with relatively well-controlled X-linked hypophosphatemia
Shintaro Senoo, Masanobu Fujimoto, Yukiko Yamaguchi, Mari Osaki, Keiichi Hanaki, Noriyuki Namba
Clin Pediatr Endocrinol. 2024; 33(1): 27–34.

Short Communication

Pitfalls in estradiol measurement by electrochemiluminescence immunoassay: A case study of a prepubertal girl with a falsely elevated serum estradiol level
Kyohei Furusawa, Rumi Hachiya, Hironori Shibata, Noboru Uchida, Goro Sasaki, Hiroyuki Fukushima, Tomohiro Ishii, Tomonobu Hasegawa
Clin Pediatr Endocrinol. 2024; 33(1): 35–38.

Mutation-in-Brief

A novel missense variant of FGD1 disrupts critical cysteine residues of the FYVE domain in Japanese siblings with Aarskog–Scott syndrome
Ikuko Takahashi, Atsuko Noguchi, Daiki Kondo, Yoko Sato, Hisato Suzuki, Mamiko Yamada, Kenjiro Kosaki, Tsutomu Takahashi
Clin Pediatr Endocrinol. 2024; 33(1): 39–42.