Category: Case Report

December 31, 2023

Genetics Corner: A New Case of Rubinstein-Taybi Syndrome with a Novel Variant in the CREBBP Gene Detected through Whole Exome Sequencing
December 31, 2023

Fellows Column: Early Identification of PURA Syndrome in a Neonate: Implications on Diagnosis and Management
December 31, 2023

Case Report: A Review of Neonatal Lupus Erythematosus with a Case Illustration
November 30, 2023

Nucleated Red Blood Cells and the Timing of Hypoxic Ischemic Encephalopathy
November 30, 2023

Genetics Corner: An infant with a CHARGE-like syndrome and dual diagnoses: Xq28 duplication and Exon 38/39 KMT2D Missense Variant syndrome
November 30, 2023

Surfactant Redosing
October 31, 2023

A Newborn with Difficult Intubation Diagnosed with Treacher Collins Syndrome and Detection of a Novel Pathogenic Variant in TCOF1
September 30, 2023

Therapeutic Hypothermia: A Hot Legal Topic
February 28, 2023

Fellow’s Column: Diagnostic and Treatment Challenges in Multisystem Inflammatory Syndrome in Neonates (MIS-N): A Success Story with Anakinra
January 31, 2023

Genetics Corner: Familial Duodenal Atresia Due to Feingold Syndrome
December 31, 2022

Genetics Corner: Mild Expression of COL7A1-Associated Epidermolysis Bullosa in a Mother and Child
August 31, 2022

Briefly Legal: Loss of Leg Secondary to an Umbilical Arterial Catheter
July 31, 2022

Clinical Pearl: Persistent Pulmonary Hypertension of the Newborn and Possible Premature Ductal Closure with History of In Utero Exposure to a Selective Serotonin Reuptake Inhibitor
June 30, 2022

It Was Worse Than Open-Heart Surgery
June 30, 2022

A Decade of Sepsis Cases in a Level III Neonatal Intensive Care Unit: An Observational Study