Hyper IgM syndrome, presentation of a clinical case in a patient from the Hospital Infantil de Tlaxcala
Introduction: Hyper-IgM syndrome is an inborn error of immunity that predisposes to […]
Case report
AUTOIMMUNITY IN A PATIENT WITH GENETIC DEFECT IN NEUROG3. CASE REPORT
Defects in NEUROG3 cause an autosomal recessive disorder characterized by intestinal malabsorption
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Menke-Hennekam Syndrome affecting an 8-year-old female child: Case Report
Introduction: Menke-Hennekam Syndrome is a novel and rare type of congenital generalized
Menke-Hennekam Syndrome affecting an 8-year-old female child: Case Report Read More »
Choreoathetosis: A Rare Manifestation of Hyper-IgM Syndrome (CD40 ligand deficiency). Case report
Hyper-IgM (HIGM) is an inborn error of immunity primarily caused by genetic
