Letter to the Editor
Original Article
Relationships between Continuous Glucose Monitoring-Derived Glycemic Parameters and Early Retinal Vascular Changes in Children with Type 1 Diabetes Mellitus
Bediz Özen, Hakan Öztürk, Emrullah Arslan, et al.
Long-Term Results of Long-Acting Somatostatin Analog Therapy in Children with Congenital Hyperinsulinism
Amine Aktar Karakaya, Edip Unal, Funda Feryal Taş, et al.
Differential Impact of Type 1 Diabetes on Bone Outcomes in Children
Sarah Wing-yiu Poon, Jianfang Zhu, Gloria Shir-wey Pang, et al.
Risk Factors for Cerebral Edema in Pediatric Diabetic Ketoacidosis: a Systematic Review and Meta-Analysis of Observational Studies
Luis Gabriel Rocha, Rayzha Kruzhkaya Cuellar, Liuba Alexandra Vargas, et al.
The Role of Sex Steroids, Sex Hormone-binding Globulin and Leptin in the Development of Pubertal Gynecomastia and its Persistence into Adulthood
Zdravka Petrova Todorova, Blagomir Nikolaev Zdravkov
Evaluation of Muscle Mass and Strength in Children and Adolescents with Disorders of Sex Development
Kürşat Çetin, Zeynep Donbaloğlu, Yasemin Funda Bahar, et al.
Case Report
Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding
Leyla Gizem Bolaç Özyılmaz, Ertuğrul İnan, Sezin Canbek, et al.
Off-Label Use of Teriparatide for Osteotomy Healing in an Adolescent with Osteogenesis Imperfecta Type VIII: A Case Report
Aylin Günay, Sare Betül Kaygusuz, Ahmet Hamdi Akgülle, et al.
Revisiting the Association of Central Precocious Puberty with Neurovisceral Diseases owing to a Girl with Niemann-Pick Disease Type C
Zümrüt Arslan Gülten, Burçin Nazlı Karacabey, Bilge Aydın Behram, et al.
Prolactinoma Associated with L-Dopa–Resistant Hyperprolactinemia in a Child with Tetrahydropterin (BH4) Deficiency
Fatma Özgüç Çömlek, Hümeyra Yaşar Köstek, Emine Dilek, et al.
Neonatal Cholestasis Caused by Graves' Disease: A Case Report and Literature Review
Yanhui Zhang, Lianshuang Liu, Yi Lu, et al.
Early-Onset Multiple Necrobiosis Lipoidica in a Child with Type 1 Diabetes Mellitus
Emel Gül Açıkgöz, Özge Yanık, Şeyma Koca, et al.
Case Reports: Exploring the Varied Presentations and Clinical Features of Carney Complex, A Detailed Report on Three Distinct Cases
İlayda Altun, Hande Turan, Aydilek Dağdeviren, et al.
Late-Onset and Recurrent Agranulocytosis During Low-Dose Methimazole Therapy in an Adolescent with Graves’ Disease
Betül Demircan Coşkun, Şebnem Yılmaz, Balahan Bora, et al.
An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused by RIT1 Mutation
Şafak Demirtaş, Elif Özsu, Zeynep Şıklar, et al.
Primary Adrenal Insufficiency in Pseudo-Neonatal Adrenoleukodystrophy Case Report
İhsan Turan, Fatma Derya Bulut, Leman Damla Kotan, et al.
A 13-Year-Old Girl with Congenital Hyperinsulinemic Hypoglycemia Due to an ABCC8 Mutation and Recent Onset of Diabetes Mellitus: A Case Report and Literature Review
Aikaterini Kantzavelou, Ekaterini Siomou, Anny Mertzanian, et al.
Short Stature and Growth Hormone Deficiency in POMC Deficiency: An Unexpected Clinical Association
Uğur Cem Yılmaz, Deniz Özalp Kızılay, Damla Gökşen, et al.
Striking Scrotal Hyperpigmentation as an Early Clinical Sign of Familial Glucocorticoid Deficiency Type 2: A Case with Homozygous MRAP Variant
Gözde Gürpınar, Duygu Gamze Aracı, Yakup Karakurt
Severe Familial Hypertriglyceridemia in a Child with Compound Heterozygous Pathogenic APOA5 Variants: A Case Report and Therapeutic Challenge
Nikola Ilić, Jovana Krstić, Dimitrije Cvetković, et al.
A Novel Biallelic Variant in The SERPINH1 Gene in Two Siblings Diagnosed with Osteogenesis Imperfecta Type X: Evidence of Intrafamilial Clinical Variability
Akçahan Akalın, İsmet Rezani Toptancı, Şervan Özalkak, et al.
FKBP10 Variants: Differentiation Between Bruck Syndrome Type 1 And Osteogenesıs Imperfecta Type XI
Gülümay Vural Topaktaş, Berna Eroğlu Filibeli, Hakan Birinci, et al.
A Rare Cause of Sacral Insufficiency Fracture in Adolescence: Autosomal Dominant Hypophosphatemic Rickets due to Fgf23 de novo P.Arg176trp Variant
Emel Hatun Aytaç Kaplan, Melih Civan, Aydeniz Aydın Gümüş, et al.
Coexistence of T1DM and GCK-MODY: Case Report and Literature Review
Yurong Piao, Congli Chen, Yuqi Miao, et al.
Symptomatic Hypercalcemia with Vomiting in a Pediatric Patient with Graves’ Disease
Goo Lyeon Kim, Kunsong Lee, Ju-Hee Seo, et al.
The Opposite Phenotype of Sotos Syndrome: 5q35.2q35.3 Microduplication Syndrome
Kübra Şen Küçük, Aydan Mengübaş Erbaş, Zehra Manav Yiğit, et al.
A Novel THRβ Variant in a Child With Resistance to Thyroid Hormone β: Diagnostic and Therapeutic Challenges
Gözde Gürpınar, Duygu Gamze Aracı
18p Deletion Syndrome Associated with Type 1 Diabetes and Hashimoto’s Thyroiditis: A Case Report on Autoimmune Disorders and Genetic Factors
Mehmet Ali Oktay, Elif Tuğçe Tunca Küçükali, Aylin Kılınç Uğurlu, et al.
A Case of CHARGE Syndrome with a Novel Intronic Variant in the CHD7 Gene
Eda Kaya, Emine Çamtosun, İsmail Dündar, et al.
Osteogenesis Imperfecta with Pes Equinovarus: A Rare Combination and a Rare Col1a1 Variant
Nurhan Özcan Murat, Yasemin Alanay
Two Countries, One Metabolic Dilemma: Nutritional Management of Concurrent Maple Syrup Urine Disease and Type 1 Diabetes Mellitus
Pınar Kılıçdağı Çanakcı, Marta Suárez Gonzále, Engin Köse, et al.
Development of Dysplastic Nevi in a Child with LEPR Deficiency Treated with Setmelanotide
Hatice Nursoy, Yasemin Denkboy Öngen, Ferdi Öztürk, et al.
A Case of Secondary Pseudohypoaldosteronism in a Neonate not Due to Urinary Tract Issues
Ecem İpek Altınok, Yavuz Özer
Diazoxide and Continuous Glucose Monitoring as Treatment in a Neonate with Hyperinsulinemic Hypoglycemia due to HNF4A Mutation
Georgia Sotiriou, Stilianos Xinias, Valentina Diamantidou, et al.
Case Report: Hypoinsulinaemic Hypoketotic Hypoglycaemia Due to an Activating Variant in AKT2
Laura Sayol-Torres, Ariadna Campos-Martorell, Julia Sala-Coromina, et al.
A Case of Adolescent Girl with Hypercalcemia Resistant to Medical Treatment Due to Giant Breast Fibroadenoma
Kürşat Çetin, Berna Singin, Yasemin Funda Bahar, et al.
Reversible Injection-Site Lipoatrophy Induced by Long-Acting Growth Hormone (Somatrogon) in Pediatric Growth Hormone Deficiency: A Case Series
Kübra Şen Küçük, Göksel Tuzcu, Ahmet Anık
Long-term Follow-up of a Case with TBX19 Mutation, a Rare Cause of Isolated ACTH Deficiency and Literature Review
Ayşegül Ceran, Zehra Aycan, Zeynep Şıklar, et al.
Duplication in the SHOX Gene as a Rare Genetic Cause of Short Stature and/or Skeletal Abnormalities: A Clinical Report and Review of the Literature
Benay Turan, Gülçin Arslan, Tayfun Çinleti, et al.
Review
Transition of Care in X-Linked Hypophosphatemic Rickets: From Pediatric to Adult Practice- A Narrative Review
Tugce Kandemir, Firdevs Bas, Serap Turan, et al.
Association between Circulating Amino Acids and Childhood Obesity: A Systematic Review and Meta-Analysis
Yingli Si, Tingting Zhang, Xiangyu Wang
WITHDRAWN
WITHDRAWN: Triglyceride Glucose Index as a Surrogate Measure of Insulin Sensitivity in a Caucasian Pediatric Population
Valeria Calcaterra, Chiara Montalbano, Annalisa de Silvestri, et al.
