Diagnosis and treatment of children with rare hemhidrosis and pediatrician's care experience: a case report
A case of Neuro-Behçet’s disease presenting with cognitive dysfunction: a case report
Myxedema Coma in Neuronal Ceroid Lipofuscinosis Type 6: a life-threatening complication in a rare disease
Familial Birt-Hogg-Dubé Syndrome diagnosed with the rare FLCN exon 6 mutation: a case series of three related patients
Potassium Pause: A Case of Cardiac Arrest Unmasking Distal Renal Tubular Acidosis
Kikuchi-Fujimoto Disease Masquerading as Dysphagia with an Isolated Pulmonary Nodule: A Clinical Conundrum
Biomarkers in young individuals with 22q11.2 deletion syndrome, a population at high risk for dopaminergic neuropsychiatric disease
Dying Before the System Caught Up: A Case of Neurofibromatosis Type 1 in a Geriatric Patient with Pain and Polypharmacy
Isolated Cryptococcus Bloodstream Infection in a Non-HIV Patient Following Rituximab Therapy for B-Cell Lymphoma: A Therapeutic Challenge and Literature Review
CACP Syndrome: A Rare Non-inflammatory Arthropathy Often Misdiagnosed as Juvenile Idiopathic Arthritis – Clinical Insights and Diagnostic Approach