Information on IMD33

Basic details

Name: Immunodeficiency 33 | Acronym: IMD33
Alt. names:

Gene: IKBKG | MOI: X-linked recessive | Mechanism of action:

No. of cases in DB: 0 | First reported in: 2004

Last updated on: 2023-02-28 16:41:18 by

OMIM: 300636

Orphanet: -

MONDO: -

DOID: -

ClinGen:

Description

In Immunodeficiency 33 (Atypical mycobacteriosis), there is evidence that considerations should be taken related to certain vaccines (eg, BCG vacine should be avoided), and recognition of potential sequelae of immunodeficiency may allow prompt diagnosis and treatment of infectious manifestations; In Immunodeficiency 33, in addition to vaccine-related considerations, treatment with IVIG has been reported as beneficial; In Ectodermal dysplasia, anhdyrotic/hypohidrotic, with immune deficiency, prophylactic measures relating to infectious complications, (eg, IVIG and antibiotics) have in some individuals been described as improve clinical status when initiated early, and prompt and aggressive treatment of infections may be beneficial; In Isolated immunodeficiency, antiinfectious prophylaxis and early and aggressive treatment of infections may be beneficial; In Incontinentia pigmenti, type II, which may be clinically recognizable, fluorescein angiography has been recommended in order to diagnose ischemic retina in individuals with retinal changes, and early treatment with peripheral retinal photocoagulation may reduce the risk of retinal detachment; In IKBKG-related immunodeficiency such as Invasive pneumococcal disease, antiinfectious prophylaxis and early and aggressive treatment of infections may be beneficial; HSCT has been described in Ectodermal dysplasia and immunodeficiency 1. In Ectodermal dysplasia, anhdyrotic/hypohidrotic, with immune deficiency, some individuals have been described as not responding well to preventive measures/treatment; Lung transplantation has been described. Refs. PMIDs: 117248; 8923006; 10839543; 11047757; 11590134; 11242109; 11224521; 11241484; 12588226; 15577852; 15356572; 16228229; 16333836; 16532398; 16818673; 16950813; 20301645; 20829317; 21993693; 22453515; 28993958; 29534156; 30422821; 31965418

Management

Description of management option has not been reviewed yet.

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0 reported cases added to GenIA

SubjectID Sex Fam.ID AD AFM Validity Country Population Reference & Pub.code

AD: Age at genetic diagnosis; AFM: age at first manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).

Summary of clinical findings

[Considering only Definitive and Possible cases]

Rank Clinical term Present Absent Unreported
1 Conical tootharrow icon 4 (80.0%) 0 (0.0%) 1 (20.0%)
2 repeated bacterial infectionsarrow icon 2 (99.9%) 0 (0.0%) 0 (0.0%)
3 Decreased IgM levelsarrow icon 1 (50.0%) 0 (0.0%) 1 (50.0%)
4 Hypodontiaarrow icon 1 (33.3%) 0 (0.0%) 2 (66.7%)
5 Immunodeficiencyarrow icon 1 (99.9%) 0 (0.0%) 0 (0.0%)
6 Increased IgA levelsarrow icon 1 (50.0%) 0 (0.0%) 1 (50.0%)
7 Infantile onsetarrow icon 1 (99.9%) 0 (0.0%) 0 (0.0%)
8 Pneumocystis jiroveci pneumoniaarrow icon 1 (99.9%) 0 (0.0%) 0 (0.0%)
9 Delayed eruption of teetharrow icon 0 (0.0%) 0 (0.0%) 1 (99.9%)

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Summary of treatment outcomes

[Considering only Definitive and Possible cases]

Treatment ⓘ Responses & clinical indications

Please mind that full curation of this condition has not started yet. Please contact us if you want to volunteer.