Review

Adipocytokine profiles in maternal obesity: The impact of lipoinflammation on serum, breastmilk, and infant metabolic development
Mario Daniel Caba-Flores, Cesar Huerta-Canseco, Carmen Martínez-Valenzuela, Aurora de Jesús Garza-Juárez, Ana María Rivas-Estilla, Alberto Camacho-Morales
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 204–212.

Original Articles

Utility of the FT3-to-FT4 ratio as a screening marker for pediatric Graves’ disease
Kazuhiro Shimura, Kentaro Sawano, Keisuke Nagasaki, Kiyomi Abe, Tomohiro Ishii, Tomonobu Hasegawa, Yukihiro Hasegawa
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 213–218.

Onset of puberty in boys with short stature is earlier in those born small-for-gestational age and later in those born appropriate-for-gestational age than in the general healthy population
Kentaro Kishi, Shun Soneda, Takahiro Mochizuki, Masahiro Noda, Naoko Sato, Toshiaki Tanaka
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 219–225.

Japanese growth charts stratified by birth weight in 500-gram increments: Findings from the Japan Environment and Children’s Study
Takeshi Yamaguchi, Naomi Tamura, Hiroyoshi Iwata, Sachiko Itoh, Mariko Itoh, Maki Tojo, Keitaro Makino, Yasuaki Saijo, Akie Nakamura, Yoshiya Ito, Kazutoshi Cho, Akinori Moriichi, Yumi Kono, Taro Yamauchi, Reiko Kishi, for the Japan Environment and Children’s Study Group
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 226–239.

Case Reports

A 14-yr-old boy with a pathogenic MEN1 variant was diagnosed with asymptomatic insulinoma during routine follow-up
Risa Yokoyama, Takumi Shibazaki, Chizuko Nakamura, Haruka Morota, Yozo Nakazawa
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 240–248.

A Japanese infant with fulminant type 1 diabetes with disease-sensitive CSAD polymorphism and HLA haplotype
Junko Kanno, Hirohito Shima, Miki Kamimura, Akiko Saito-Hakoda, Atsuo Kikuchi
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 249–253.

Double ‘A’ phenotypes with mineralocorticoid deficiency: A rare presentation of Allgrove syndrome
Arindam Ghosh, Saba Annigeri, Chakita Singh, Sunil Kumar Hemram
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 254–259.

KCNJ11 readthrough variant in a patient with congenital hyperinsulinism
Erika Uehara, Keiichi Sugihara, Ikue Hata, Kazuhisa Akiba, Atsushi Hattori, Ikuko Kageyama, Keiko Matsubara, Maki Fukami
Clin Pediatr Endocrinol. 2025 Jul; 34(4): 260–263.

Neonatal hyperthyroidism in an extremely low birth weight infant born to a mother with Graves’ disease
Daly Pen, Kimyi Phou, Sokuntheavy Ly, Rathmony Heng, Sakviseth Bin, Sethikar Im
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 264–267.

Van Wyk–Grumbach syndrome: a case report and review of the literature
Yosuke Komatsu, Nobuyuki Kikuchi
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 268–274.

Short Communication

A case of autosomal dominant hypophosphatemic rickets
Shigeru Takishima, Kei Takasawa, Nozomi Matsuda, Hisae Nakatani, Kenichi Kashimada
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 275–279.

Mutation-in-Brief

COL10A1-related metaphyseal dysplasia Schmid caused by the p.L644F variant in the COL10A1 gene
Tomoyuki Ito, Yurika Senoo, Takahiro Shindo, Yoshiyuki Namai, Yoichiro Oda
Clin Pediatr Endocrinol. 2025 Oct; 34(4): 280–283.