Case Report

O2054: Wandering Spleen Presenting as an Ileus in a Pediatric Patient: A Case Report

O2056: Not Just a chunk: Mitral and aortic Valve Infective Endocarditis caused by Abiotrophia Defectiva

O3200: Thalami and Dentate Nuclei Involvement in an Infant with Propofol Related Infusion Syndrome

O3201: Seizing the Opportunity: An Incontinentia Pigmenti Case Report

O3204: Mandibular arteriovenous malformation: a rare but serious diagnosis

O3209: EBV Infection Presenting with Concurrent Encephalitis and GBS in an Immunocompetent Adolescent

O3229: Goldilocks Grief: Provider Expectations and Response to Caregiver Grief Response in the PICU

P2.A011: Difficulties navigating cultural, religious, and parental differences at end of life in adolescent and young adults: A case report

P2.A012: Diffuse alveolar hemorrhage in the setting of chronic opioid inhalation

P2.C049: Outcome of a 4-Year-Old Male with Febrile Infection-Related Epilepsy Syndrome: A Case Report

P2.C051: A pediatric case of Bickerstaff's Brainstem Encephalitis with relapse of symptoms following initial treatment with IVIG and steroids.

P2.C052: Complications of Acute Chest syndrome and Septic Shock in a Pediatric Sickle Cell Patient requiring ECMO

P2.C056: Diffuse Alveolar Hemorrhage Secondary to Non-Prescribed Fentanyl Overdose in a Young Child

P2.C057: The Vital Role of Early Symptom Identification and Aggressive Management in Preventing Fatal Outcomes: Autoimmune Polyglandular Syndrome Case Report

P2.C058: Rapid Neurological Deterioration in an Adolescent Female due to Myelin Oligodendrocyte Glycoprotein Antibody Disease, a Case Report

P2.C059: Calcium channel and beta blocker intoxication: A management challenge in an overmedicated psychiatric patient.

P2.C060: Atypical Laboratory Findings in DKA with Cannabis Use

P2.D062: Oral N-Acetylcysteine Use for Acetaminophen Toxicity in an Infant

P2.K211: A Beacon of Hope: Innovative Management of Febrile Infection-Related Epilepsy Syndrome (FIRES) with Intrathecal Steroids

P2.K212: A Rare Cause of Short-Rib Thoracic Dysplasia in a Neonate

P2.K213: A Rare Encounter: Intraductal Papilloma Presenting as a Breast Mass in an 8-Month-Old Male

P2.K214: Atypical Congenital Pancreatic Abnormality Causing SMA-like Syndrome in a Pediatric Patient

P2.K215: Atypical Presentation of Kawasaki Disease: A Case Report

P2.K216: Bowel dilation and its impact on menstruation: a rare complication of Hirschsprung Disease

P2.K217: Bullous IgA Vasculitis: A Unique Presentation and Potential Marker of Severity

P2.K218: Cervical Spine Arthritis as a Manifestation of Kawasaki Disease

P2.K219: Consider Acute Disseminated Encephalomyelitis in a Child with Acute Neurological Deficits

P2.K220: Constipation in a Three Year Old: Common Symptom, Uncommon Disease

P2.L221: Deciphering Kawasaki Disease: Lymphadenopathy as a Diagnostic Conundrum

P2.L222: Diagnosing Failure to Thrive: A Case of 22q11.2 Deletion Syndrome in Identical Twins

P2.L223: Discovering the Unknown: Adolescent with Dilated Cardiomyopathy with Severe Acquired Hypothyroidism

P2.L224: Dysphagia, bradypnea and bradycardia: Have you considered the cerebellum?

P2.L225: Eczema, Eczema, Eczema… Kwashiorkor?

P2.L226: Haemophilus parainfluenzae urinary tract infection and bacteremia in 38-day-old male with structural ureteral abnormality

P2.L227: HIV/AIDS as Mimicker of Inflammatory Bowel Disease

P2.L228: Incidental hepatosplenomegaly leads to a rare diagnosis of autoimmune lymphoproliferative syndrome

P2.L229: Intracranial Calcifications in an Adolescent: A Case Report

P2.L230: Invasive Pneumococcal Meningitis Susceptible but Not Responsive to Ceftriaxone

P2.L231: Isles of White in a Sea of Red: A Case Report on Dengue Fever Complicated by Hemophagocytic Lymphohistiocytosis

P2.L232: Kidneys on the loose: three cases of pediatric intrathoracic kidney and co-existing Bochdalek hernia

P2.L233: Looking Past the Interference: Toddler with Persistent Fever, Rash, and Lymphadenopathy

P2.L234: Migrainosus Misadventure, A Crisis in Disguise

P2.L235: Milky Blood: An Unusual Finding in an Infant with Rectal Bleeding

P2.L236: Myositis and Encephalopathy as Presenting Symptoms in Murine Typhus

P2.L237: Nasal Polyps Leading to Newly Diagnosed Cystic Fibrosis in an Adolescent

P2.L238: Navigating the Labyrinth: Unveiling Rare Paths in Neonatal Overgrowth and the Odyssey of Novel Interventions

P2.L239: Neonatal Onset Multisystem Inflammatory Disease Presenting as an Urticarial Rash in a Newborn

P2.L240: Neurologic evaluation of megalencephaly- postaxial polydactyly- polymicrogyria- hydrocephalus (MPPH) syndrome in a neonate

P2.M241: Non-Hodgkin Lymphoma Presenting as Abdominal Pain in an Adolescent Female

P2.M242: Not Just Sjögren's: A Unique Presentation of Macrophage Activation Syndrome

P2.M243: Novel Presentation of Invasive Group A Streptococcus Infection in a Pediatric Patient

P2.M244: Now you see me, now you don't: a toddler's tale of vision loss

P2.M245: Nutritional Deficiencies in Children with Autism Spectrum Disorder-Related Food Selectivity: Implications for the Pediatric Hospitalist.

P2.M246: On the Dot; Repetitive Episodes of Urticaria in a Neonate on Total Parenteral Nutrition (TPN).

P2.M247: Pasteurella Multocida empyema from canine kisses: A rare case of Pasteurella meningitis in a 9-month-old infant complicated by empyema.

P2.M248: Pediatric Stroke Complicated by Meningitis and Ventriculomegaly: A Case Study of Early Intervention and Complex Management

P2.M249: Pneumocephalus and Meningitis in a Previously Healthy Female

P2.M250: Rethinking Rett: Unveiling the XY Factor

P2.M251: Ricochet: Case of a Foreign Body Folly​

P2.M252: Seizures in an Exclusively Breastfed 10-Month-Old Infant

P2.M253: Septic Shock and Pancytopenia Associated with Parvovirus B19

P2.M254: Small Vessels, Big Impact: A Patient with Granulomatosis with Polyangiitis

P2.M255: Spastic left colon syndrome after long-term, high-volume antegrade continence enema use

P2.M256: The “Missing Link” In A Case Of Mastoiditis

P2.M257: The Disease of 1000 Faces: A Case Report of Multisystem Progression of Systemic Lupus Erythematosus

P2.M258: Transmission of vaccine-strain varicella zoster virus from an immunocompetent mother to an infant causing disseminated varicella

P2.M259: Trust Your Gut: When Intussusception Requires Bowel Resection in Henoch-Schönlein Purpura

P2.M260: Unraveling Hypogenetic Lung Syndrome with a Bronchogenic Cyst in a 3-Week-Old Infant with Respiratory Distress

P2.N261: Urinary tract infection caused by Gardnerella vaginalis in a 6 week old infant

P2.N262: Urine Trouble: An A-stone-ishing Case of Abdominal Pain

P2.N263: We Gave it a Shot: Streptococcus Pneumoniae Meningitis in a Fully Vaccinated Adolescent

P2.N264: Where is the pneumonia? A child with isolated pleural effusion secondary to tuberculosis.

P2.Q334: Identifying Id Reaction: A Case of an Autoeczematization after Bullous Tinea

P3.B029: Dermatologic Symptoms as Primary Manifestation of Syphilis: A Case Report

P3.B034: Marijuana-Induced Seizures in a 4-Month-Old: A Unique Presentation Requiring Child Protection Team Evaluation.

P3.B035: More than skin deep- A delayed case of non accidental trauma in a pediatric patient

P3.B036: Slipping Through the Cracks: Reporting Sentinel Injuries Is Not Always Enough

P3.G136: "A Misfortunate Pair”: Tuberculous and Cryptococcal Meningitis Co-infection in an Immunocompetent Child

P3.G137: A Global Health Threat in the Southern Border Region: A Case of Pediatric Tuberculosis Meningitis in an International Patient Complicated by a Recent Paternal Loss

P3.G138: Clinical Presentation and Management of PHACE Syndrome in a Pediatric Patient: A Case Report

P3.G139: Consumed by Consumption: Diagnostic and Treatment Challenges in a Case of Pediatric Disseminated Tuberculosis

P3.G140: Pediatric Autoimmune Encephalitis: Navigating Limitations for Optimal Prognosis in Resource-Limited Settings

P3.G141: Status Epilepticus Secondary to Intracranial Tuberculomas in a Child with Relapsed Familial HLH and Griscelli Syndrome

P3.H142: Who let the dogs out?: A Case of Pneumonia Associated With Pulmonary and Hepatic Hydatid Disease from Ecuador

P3.I167: An Apple a Day Keeps the Doctor Away: Symptomatic Management of Persistent Hiccups in a Patient Undergoing Hematopoietic Stem Cell Transplant

P3.I169: Employing Primary Palliative Care Skills in Treatment of Hospitalized Patients with Anorexia Nervosa

P3.M241: A Case of Juvenile Mixed Connective Tissue Disorder(MCTD) in a Young Female: A Wolf in Sheep's Clothing.

P3.M242: Acute appendicitis in an infant: Case report

P3.M243: Beyond a Sprain: An Unusual Presentation of Bone Pain in a 16 -year-old Male

P3.M244: Beyond the Bulge: An Unusual Case of Proptosis in an Infant

P3.M245: Brain Abscess Positive for Streptococcus pneumoniae in an 11-Year-Old Female Attributable to Inadequate Treatment of Otitis Media

P3.M246: Case Report: Identification of Multiple Small Intestinal Arteriovenous Malformations with Double Balloon Enteroscopy in a Pediatric Patient.

P3.M247: Chronic Suppurative Otitis Media due to Aspergillus, Pseudomonas, and MRSA in the Setting of Immunodeficiency and Adverse Drug-Reactions

P3.M249: Decline in gut motility in cerebral palsy patients after triggering event: a discussion on invasive versus conservative management

P3.M255: Exploring Pediatric Colonic Volvulus: A Case Study and Diagnostic Considerations

P3.M256: GATA-2 Deficiency Unveiled: A Multifaceted Presentation in an Adolescent with Mycobacterial Infection and Pulmonary Alveolar Proteinosis

P3.M257: Identification of an EWSR1-BEND2 Fusion-Positive Pediatric Gastric Tumor through RNA Sequencing: A Case Report

P3.M258: ImmunoCrossroads: The Role of Med-Peds and the Intersection of Autoimmune Disorders

P3.N262: Intestinal Failure Associated With Liver Disease and the use of Fish Oil: A Case Report

P3.N263: Kugulberg Walender Syndrome, Spinal Muscular Atrophy SMA Type 3, A Diagnostic Challenge

P3.N265: Nephroptosis – a rare but potentially serious complication in renal transplant recipients

P3.N266: Not just dry eyes and dry mouths: Sjögren's syndrome in a young adult presenting with severe hypokalemia and kidney stones

P3.N267: Pain Relief or Painful Twist? NSAID-Induced Aseptic Meningitis in an Adolescent Patient

P3.N268: Paraganglioma in a Pediatric Patient: Case Report

P3.N269: Pediatric Wegener’s Granulomatosis: A Case Study Highlighting Diagnostic and Management Hurdles

P3.N272: Relapsed bacterial meningitis in an adolescent patient with aberrant patent foramen caecum

P3.N273: Severe dengue mimicking Kawasaki disease in an infant: a case report.

P3.N274: Teenager with Hennekam Syndrome

P3.N277: When Cushing's Syndrome Reveals A Wilms' Tumor: Impact Of Ectopic ACTH Production.

P3.N278: When too much weight loss went wrong – Median arcuate ligament syndrome in a teenager after rapid weight loss

P3.Q324: A Rapid Progression of Amebic Meningoencephalitis

P3.Q329: Twists and Turns: Ovarian Torsion Unveiled in an Infant

P3.R353: Sternoclavicular joint dislocation: a shoulder injury you shouldn’t shrug off

P3.R354: “Take Me Out of the Ballgame” A Case of Acromial Apophysiolysis in a High School Softball Pitcher

P3.R355: Hip Pain as a Manifestation of Pediatric Endocarditis: A Case Report

P3.R357: Ischiopubic stress injury in a 9 year old baseball player: A Case Report

P3.R358: Thoracic Outlet Syndrome in a Teenage Softball Pitcher: A Rare Presentation of Biceps Pain

P3.R359: Avascular Necrosis of the Hip in a Basketball Player

P3.S370: Neuronal migration defects and infantile spasms in mosaic partial tetrasomy of chromosome 3q

P3.S371: CFTR and Pediatric Chronic Pancreatitis

P3.S372: Fever, Otorrhea and Discomfort with Valsalva: An Unusual Presentation of Neonatal E. coli Infection

P3.S378: First Do No Harm: High Risk HPV in a 15yo Female

P3.S379: Focal Nodular Hyperplasia Mimicking Relapse in Wilms Survivor

P3.T384: More Than Skin Deep: A case of DRESS Syndrome Highlighting the Importance of Rash Evaluation in Dark Skinned Individuals

P3.T388: The Dermato-Fight: A Curious Rash Following Tropical Travel

P3.T390: Toddler with Hypoxemic Respiratory Failure

P4.A009: Mosaic Intersectin-1 gene related neurodevelopmental disorder: A case report