Information on DKCA2

Basic details

Name: Dyskeratosis congenita, autosomal dominant 2 | Acronym: DKCA2
Alt. names:

Gene: TERT | MOI: Autosomal dominant | Mechanism of action:

No. of cases in DB: 0 | First reported in: 2005

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

OMIM: 613989

Orphanet: -

MONDO: -

DOID: -

ClinGen:

Description

In dyskeratosis congenita, the presentation many not always be classic, and individuals are at high risk for hematologic anomalies (including bone marrow failure) and malignancy, and surveillance and prompt diagnosis and treatment may be beneficial; In Aplastic anemia, surveillance and prompt treatment of aplastic anemia and bone marrow failure may reduce morbidity; HSCT may be effective; For treatment related to pulmonary fibrosis, immunotherapy may be beneficial, though lung transplantation may be indicated in individuals with severe/refractory disease. Refs. PMIDs: 16247010; 15814878; 16890917; 17392301; 17785587; 17460043; 18460650; 18042801; 19760749; 21602826; 20502709; 21436073; 22512499; 20301779

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 Middle age onsetarrow icon 3 (50.0%) 0 (0.0%) 3 (50.0%)
2 Osteoporosisarrow icon 3 (50.0%) 0 (0.0%) 3 (50.0%)
3 Premature graying of hairarrow icon 3 (50.0%) 0 (0.0%) 3 (50.0%)
4 Pulmonary fibrosisarrow icon 3 (50.0%) 0 (0.0%) 3 (50.0%)
5 Hepatic fibrosisarrow icon 2 (33.3%) 0 (0.0%) 4 (66.7%)
6 Thrombocytopeniaarrow icon 2 (33.3%) 0 (0.0%) 4 (66.7%)
7 White forelockarrow icon 2 (33.3%) 0 (0.0%) 4 (66.7%)
8 Young adult onsetarrow icon 2 (33.3%) 0 (0.0%) 4 (66.7%)
9 Aplastic anaemiaarrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
10 Osteonecrosisarrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
11 Juvenile onsetarrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
12 Neutropeniaarrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
13 Pancytopeniaarrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
14 short staturearrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)
15 Urethral stricturearrow icon 1 (16.7%) 0 (0.0%) 5 (83.3%)

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Summary of treatment outcomes

[Considering only Definitive and Possible cases]

Treatment ⓘ Responses & clinical indications

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