Diagnostics of rare disorders : whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

Näytä kaikki kuvailutiedot



Pysyväisosoite

http://hdl.handle.net/10138/243577

Lähdeviite

Trotta , L , Norberg , A , Taskinen , M , Beziat , V , Degerman , S , Wartiovaara-Kautto , U , Välimaa , H , Jahnukainen , K , Casanova , J-L , Seppänen , M , Saarela , J , Koskenvuo , M & Martelius , T 2018 , ' Diagnostics of rare disorders : whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders ' , Orphanet journal of rare diseases , vol. 13 , 139 . https://doi.org/10.1186/s13023-018-0864-9

Julkaisun nimi: Diagnostics of rare disorders : whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders
Tekijä: Trotta, Luca; Norberg, Anna; Taskinen, Mervi; Beziat, Vivien; Degerman, Sofie; Wartiovaara-Kautto, Ulla; Välimaa, Hannamari; Jahnukainen, Kirsi; Casanova, Jean-Laurent; Seppänen, Mikko; Saarela, Janna; Koskenvuo, Minna; Martelius, Timi
Tekijän organisaatio: Institute for Molecular Medicine Finland
Helsinki Institute of Life Science HiLIFE
University of Helsinki
Lastentautien yksikkö
Children's Hospital
Clinicum
Department of Oncology
Hematologian yksikkö
Medicum
Department of Virology
Oral and Maxillofacial Surgery
Doctoral Programme in Clinical Research
Department of Medicine
Infektiosairauksien yksikkö
Doctoral Programme in Integrative Life Science
Janna Saarela / Principal Investigator
HUS Children and Adolescents
HUS Comprehensive Cancer Center
Päiväys: 2018-08-17
Kieli: eng
Sivumäärä: 9
Kuuluu julkaisusarjaan: Orphanet journal of rare diseases
ISSN: 1750-1172
DOI-tunniste: https://doi.org/10.1186/s13023-018-0864-9
URI: http://hdl.handle.net/10138/243577
Tiivistelmä: Background: The telomere biology disorders (TBDs) include a range of multisystem diseases characterized by mucocutaneous symptoms and bone marrow failure. In dyskeratosis congenita (DKQ, the clinical features of TBDs stem from the depletion of crucial stem cell populations in highly proliferative tissues, resulting from abnormal telomerase function. Due to the wide spectrum of clinical presentations and lack of a conclusive laboratory test it may be challenging to reach a clinical diagnosis, especially if patients lack the pathognomonic clinical features of TBDs. Methods: Clinical sequencing was performed on a cohort of patients presenting with variable immune phenotypes lacking molecular diagnoses. Hypothesis-free whole-exome sequencing (WES) was selected in the absence of compelling diagnostic hints in patients with variable immunological and haematological conditions. Results: In four patients belonging to three families, we have detected five novel variants in known TBD-causing genes (DKC1, TERT and RTEL1). In addition to the molecular findings, they all presented shortened blood cell telomeres. These findings are consistent with the displayed TBD phenotypes, addressing towards the molecular diagnosis and subsequent clinical follow-up of the patients. Conclusions: Our results strongly support the utility of WES-based approaches for routine genetic diagnostics of TBD patients with heterogeneous or atypical clinical presentation who otherwise might remain undiagnosed.
Avainsanat: Telomere biology disorders
Telomeropathies
Next-generation sequencing
Whole-exome sequencing
Dyskeratosis congenita
DKC1
TERT
RTEL1
HOYERAAL-HREIDARSSON SYNDROME
BURROWS-WHEELER TRANSFORM
DYSKERATOSIS-CONGENITA
MOLECULAR-GENETICS
READ ALIGNMENT
MUTATIONS
VARIANTS
3121 General medicine, internal medicine and other clinical medicine
3111 Biomedicine
Vertaisarvioitu: Kyllä
Tekijänoikeustiedot: cc_by
Pääsyrajoitteet: openAccess
Rinnakkaistallennettu versio: publishedVersion


Tiedostot

Latausmäärä yhteensä: Ladataan...

Tiedosto(t) Koko Formaatti Näytä
s13023_018_0864_9.pdf 752.1KB PDF Avaa tiedosto

Viite kuuluu kokoelmiin:

Näytä kaikki kuvailutiedot