Pyogenic Bacterial Infections Due To Myd88 Deficiency

Description

Pyogenic bacterial infection due to MyD88 deficiency is a primary immunodeficiency characterized by increased susceptibility to pyogenic bacterial infections, including invasive pneumococcal, invasive staphylococcal and pseudomonas disease.

Clinical Features

Phenotypes and symptoms related to Pyogenic Bacterial Infections Due To Myd88 Deficiency

  • Fever
  • Immunodeficiency
  • Recurrent bacterial skin infections

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Pyogenic Bacterial Infections Due To Myd88 Deficiency Is also known as myd88 deficiency, pyogenic bacterial infections, recurrent, due to myd88 deficiency, recurrent pyogenic bacterial infections due to myd88 deficiency.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Pyogenic Bacterial Infections Due To Myd88 Deficiency Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MyeloidDx by NGS.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).

RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, FBXW7, CDKN2A, PHF6, ASXL1, CEBPA , (...)

View the complete list with 32 more genes
Specificity
2 %
Genes
100 %
MyeloidDx by NGS.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).

RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, CBLC, FBXW7, CDKN2A, PHF6, CEBPA , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
100 %
MYD88 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

MYD88
Specificity
100 %
Genes
100 %
MYD88 Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

MYD88
Specificity
100 %
Genes
100 %
Waldenström macroglobulinemia (p.Leu265Pro mutation on MYD88 gene).

By CGC Genetics (Portugal).

MYD88
Specificity
100 %
Genes
100 %
Myeloid Tumor Panel.

By Centogene AG - the Rare Disease Company (Germany).

RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, CBLC, FBXW7, CDKN2A, PHF6, ASXL1 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
100 %
Macroglobulinemia, Waldenstrom, somatic.

By Centogene AG - the Rare Disease Company (Germany).

MYD88
Specificity
100 %
Genes
100 %
Pyogenic bacterial infections, recurrent, due to MYD88 deficiency.

By Centogene AG - the Rare Disease Company (Germany).

MYD88
Specificity
100 %
Genes
100 %

You can get up to 24 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM ORPHANET Rare Disease Symptoms Checker

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