Previous Issue   Volume 28(Suppl 1); Dec 2023
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Mixed diabetic ketoacidosis and hyperglycemic hyperosmolarity in a girl with nephronophthisis 4 presenting with rhabdomyolysis and pancreatitis
Eu-Seon Noh, Chiwoo Kim, Sung Yoon Cho
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S1-S2.
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Maturity-onset diabetes of the young due to NR0B2 gene mutation
Hae In Lee, Soon Sung Kwon, Myeongseob Lee, Su Jin Kim, Kyungchul Song, Ahreum Kwon, Hyun Wook Chae, Ho-Seong Kim, Junghwan Suh
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S3-S5.
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A Korean child with DICER1 syndrome presenting with thyroid manifestations accompanied by other types of neoplasms: a case report and literature review
Minji Kim, Jun Lee, Sukdong Yoo, Ji Yeon Song, Eu Jeen Yang, Seong Heon Kim, Chong Kun Cheon, Ju Young Yoon
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S6-S8.
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Case report of familial hypobetalipoproteinemia: a novel APOB mutation and literature review
So Yun Park, Heung Sik Kim, Mi Ae Chu, Hyo-Jeong Jang, Seokjin Kang
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S9-S11.
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A Korean boy with a CHD8 mutation who presented with overgrowth, intellectual disability, and autism
Chiwoo Kim, Eu-seon Noh, Sung Yoon Cho
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S12-S13.
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Turner syndrome due to Xp22.33 deletion combined with 7p22.3 duplication
Ha young Jo, Hyun Ji Jang, Young Mi Kim, Soo-Han Choi, Kyung Hee Park, Hye Won Yoo, Su Jeong Park, Yoon Hee Jo, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S14-S16.
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A case of type A insulin resistance syndrome in a 14-year-old adolescent girl without common clinical features
Na won Lee, Ji Eun Jeong, Young Hwan Kim, Chang Seok Ki, Jin Kyung Kim
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S17-S19.
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A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patient
Gimin Lee, Mi Seon Lee, Rosie Lee, Jung Eun Moon
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S20-S22.
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Using low-dose octreotide with diazoxide-resistant congenital hyperinsulinism resulting from compound heterozygous mutations in the ABCC8 gene
Kyujung Park, Kyung In Lim, Young Bae Sohn, Hae Sang Lee, Jin Soon Hwang
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S23-S24.
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Growth hormone deficiency in a boy with Wiedemann-Steiner syndrome: a case report and review
Mi Ra Kim, Eun-Gyong Yoo, Seonkyeong Rhie, Go Hun Seo, Mo Kyung Jung
Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S25-S28.
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