Inborn errors of immunity in Low German Mennonite communities in Mexico: a case series and narrative literature review - Report - MDSpire

Inborn errors of immunity in Low German Mennonite communities in Mexico: a case series and narrative literature review

  • By

  • Luisa Berenise Gámez-González

  • Saúl Oswaldo Lugo-Reyes

  • Rogelio Guzmán-Cotaya

  • Sara Elva Espinosa-Padilla

  • Luis Enrique Murguía-Favela

  • Marco Antonio Yamazaki-Nakashimada

  • June 24, 2026

  • 0 min

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Clinical Report: Genetic Immunity Disorders in Low German Mennonite Populations

Background

Inborn errors of immunity (IEI) are genetic disorders that lead to immune dysfunction, increasing susceptibility to infections and other health issues. The Low German Mennonite (LGM) community in Mexico is characterized by genetic isolation and a high prevalence of autosomal recessive conditions, making it a significant population for studying IEI.

Data Highlights

PatientConditionGenetic CauseTreatment
1G6PC3 deficiencyConfirmedGranulocyte colony-stimulating factor
2X-linked agammaglobulinemiaBTK gene variantImmunoglobulin replacement
3Severe combined immunodeficiency (SCID)ConfirmedHematopoietic cell transplantation
4Severe combined immunodeficiency (SCID)ConfirmedHematopoietic cell transplantation

Key Findings

  • Four patients with distinct inborn errors of immunity (IEI) were identified in LGM communities in Mexico.
  • Conditions included G6PC3 deficiency, X-linked agammaglobulinemia, and severe combined immunodeficiency (SCID).
  • All patients required disease-specific therapies, including granulocyte colony-stimulating factor, immunoglobulin replacement, and hematopoietic cell transplantation.
  • Genetic isolation in LGM communities contributes to the prevalence of rare autosomal recessive conditions.

Clinical Implications

Early diagnosis of inborn errors of immunity through newborn screening and accessible genetic testing is essential for improving patient outcomes in high-risk populations. Clinicians should consider the genetic background of patients from isolated communities when evaluating for IEI.

Conclusion

This case series enhances the understanding of inborn errors of immunity in Low German Mennonite populations and underscores the need for further research to validate these findings in larger cohorts.

Related Resources & Content

  1. Frontiers | Inborn Errors of Immunity in Low German Mennonite Communities in Mexico: A Case Series and Narrative Literature Review
  2. Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee - PMC
  3. Updated EBMT/ESID inborn errors working party guidelines for haematopoietic stem cell transplantation for inborn errors of immunity and metabolism | Bone Marrow Transplantation
  4. The Journal of Clinical Endocrinology & Metabolism — Diverse Genetic Variants and Common Clinical Features of Neuroendocrine Neoplasms in a Mexican Population
  5. Frontiers in Psychiatry — Genetic variation associated with depression in Latin American populations: a systematic review of single-nucleotide variants
  6. Frontiers in Immunology — Mendelian susceptibility to mycobacterial disease: IFN-γ-driven immunity collapse underlies heterogeneous infections
  7. Infection — A Case Study of a 38-Year-Old Female with Necrotizing Cervical Lymphadenitis Induced by Histoplasma capsulatum
  8. Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee - PMC
  9. Updated EBMT/ESID inborn errors working party guidelines for haematopoietic stem cell transplantation for inborn errors of immunity and metabolism | Bone Marrow Transplantation
  10. Frontiers | Inborn Errors of Immunity in Low German Mennonite Communities in Mexico: A Case Series and Narrative Literature Review

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