P1 |
Siblings of Laron Syndrome |
Muath Abu Abah |
P2 |
Severe Hypertriglyceridemia During Chemotherapy for Childhood Acute Lymphoblastic Leukemia |
Nasra Al Jaafari |
P3 |
Beyond Salt-Wasting CAH: The Broader Differential for a Positive Newborn Screen |
Aliya Allahwala |
P4 |
Low Bone Turnover and Intravenous Zoledronic Acid Are Insufficient to Prevent Denosumab-Induced-Rebound Hypercalcemia in Duchenne Muscular Dystrophy: A Case Report |
Fahd Alshammri |
P5 |
Serum Sickness Like Syndrome Due to Methimazole in Graves’ Disease |
Alanoud Aman |
P6 |
The Diagnostic Odyssey of Cyclical Cushing Syndrome: A Case Report |
Mary Zhao |
P7 |
Case Report of an Adolescent With Normal Breast Development, Suppressed Gonadotropins, Abnormal Ovaries, and Infantile Uterus |
Tali Baird |
P8 |
Treatment of Persistent Hypertension in a Patient With 17-Alpha-Hydroxylase Deficiency |
Laurence Bastien |
P9 |
Pediatric Cushing’s Syndrome Secondary to Ectopic ACTH Secretion by a Pancreatic Neuroendocrine Tumor: A Case Report |
Gabrielle Doré-Brabant |
P10 |
Hidden Cause of Fragile Bones: Scurvy-Induced Vertebral Compression Fractures in an Apparent Healthy 11-Year-Old—a Case Report |
Regina Duperval |
P11 |
TMEM38B Gene Mutation Associated With Osteogenesis Imperfecta |
Abdulrahman Habib |
P12 |
An Unlikely Pair-A Presentation of Hypercalcaemia and Hyponatraemia |
Annabelle Hobbs |
P13 |
Examining the Moderators of Diabetes Distress Among Adolescents With Type 1 Diabetes on the Effect of a Mindful-Self Compassion Intervention |
Alanna Jane |
P14 |
Hyperosmolar Hyperglycemic State and Significant Microvascular Complications: A Rare Presentation of Adolescent Type 2 Diabetes |
Alyssa Kahane |
P16 |
Two Siblings With Laron Syndrome and Their Response to Mecasermin Therapy. |
Elise Martin |
P17 |
Improving Tools and Clinical Processes to Identify and Address Food Insecurity |
Mara McNeil |
P18 |
The AB(C)s of Thyroid Hormone Resistance |
Mallory McNiven |
P19 |
Early Detection and Treatment of Vertebral Fractures, a Sign of Accelerated Senescence in Hutchinson-Gilford Progeria Syndrome, Is Associated With Stabilization of Vertebral Fractures |
Ulrich Montcho |
P20 |
6-Month Leuprolide Acetate for Monitoring Central Precocious Puberty Treatment Efficacy |
Rebecca Perry |
P21 |
Weight Stigma in the Pediatric Diabetes Population: Evaluating Patient Level Factors and Diabetes Related Outcomes |
Supraja Rengan |
P22 |
Primary Hyperparathyroidism Due to a Single Mutation in CDC73 in a 14-Year-Old Girl: A Case-Report |
Solène Rérat |
P23 |
Diabetes Education During Pediatric Residency Training: Are We Doing Enough? |
Gabrielle Scantlebury |
P24 |
A Case of Truly “Idiopathic” Infantile Hypercalcemia – When Calcium Is High but Everything Else Is Low |
Sulafa Sindi |
P25 |
A Case of Type 1 Diabetes Mellitus Presenting With Hypothyroidism |
Marie St Jacques |
P26 |
Not All Salt Wasting Is Congenital Adrenal HYPERplasia: Case Report of Delayed Presentation With NR0B1 Mutation |
Shwetha Suresh |
P27 |
Prevalence and Risk Factors for Bladder and Bowel Dysfunction in Children With Type 1 Diabetes |
Sruthi Thomas |
P28 |
A Description of ACTH Stimulation Testing Results in Term Neonates |
Sruthi Thomas |
P29 |
Echoes of the Past: A Case of Multiple Endocrinopathies Due to Iron Overload |
Abigail Wittenberg |
P30 |
Title: The Genetics of Mild Isolated Neonatal Hyperthyrotropinemia – an Additional Tool to Help Predict Transient vs. Permanent Congenital Hypothyroidism? |
Nicole Yokubynas |
P31 |
Unrecognized Social Needs in a Pediatric Diabetes Clinic: Insights From Navigating Social Resources for Children’s Health (NSRCH) Study |
Reem Al-Obiade |
P32 |
The Causal Role of Endocrine Disrupting Chemicals in Pubertal Timing: A Mendelian Randomization Study |
Melody Zuo |