IGKC gene related symptoms and diseases

All the information presented here about the IGKC gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to IGKC gene

Symptoms // Phenotype % Cases
Diarrhea Very Common - Between 80% and 100% cases
Recurrent infections Very Common - Between 80% and 100% cases
Recurrent respiratory infections Very Common - Between 80% and 100% cases
Respiratory tract infection Very Common - Between 80% and 100% cases
Abnormal immunoglobulin level Very Common - Between 80% and 100% cases

Rare diseases associated to IGKC gene

Here you will find a list of rare diseases related to the IGKC. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


RECURRENT INFECTIONS ASSOCIATED WITH RARE IMMUNOGLOBULIN ISOTYPES DEFICIENCY

Alternate names

RECURRENT INFECTIONS ASSOCIATED WITH RARE IMMUNOGLOBULIN ISOTYPES DEFICIENCY Is also known as selective igg subclass deficiency, igg subclass deficiency with iga subclass deficiency, kappa-chain deficiency, isolated igg subclass deficiency, kappa chain deficiency

Description

Deficiencies in immunoglobulin (Ig) isotypes (including: isolated IgG subclass deficiency, IgG sublcass deficiency with IgA deficiency and kappa chain deficiency) are primary immunodeficiencies that are often asymptomatic but can be characterized by recurrent, often pyogenic, sinopulmonary infections.

Most common symptoms of RECURRENT INFECTIONS ASSOCIATED WITH RARE IMMUNOGLOBULIN ISOTYPES DEFICIENCY

  • Diarrhea
  • Recurrent infections
  • Recurrent respiratory infections
  • Respiratory tract infection
  • Abnormal immunoglobulin level


More info about RECURRENT INFECTIONS ASSOCIATED WITH RARE IMMUNOGLOBULIN ISOTYPES DEFICIENCY

SOURCES: MESH OMIM ORPHANET


Potential gene panels for IGKC gene

Antibody deficiencies Panel Panel

Germany.

By CeGaT GmbH Antibody deficiencies Panel that also includes the following genes: BTK TCF3 TCF4 CD40 TNFSF12 CD40LG UNG AICDA BLNK RTEL1

More info about this panel
Germany.

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like BIVM-ERCC5 SOX9 SIK1 PXDN