ID

45965

Description

Principal Investigator: Jorge Di Paola, MD, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA MeSH: Thrombocytopenia,Abnormal Erythrocytes,B-Cell Leukemia https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000873 A family with a history of bleeding, variable thrombocytopenia, red cell macrocytosis and two cases of pre B-cell acute lymphoblastic leukemia was studied in a single visit. The family was assessed for bleeding history using a bleeding questionnaire. Additionally, complete blood counts were measured and whole blood was collected from five affected individuals and three unaffected individuals for DNA extraction and whole exome sequencing. The goal of this study is to determine the genetic cause of thrombocytopenia, red cell macrocytosis, and predisposition to leukemia in a family. It is hoped that the information obtained from this study will help researchers understand the genetic and molecular basis of platelet and red cell production, as well as leukemia predisposition.

Lien

dbGaP study=phs000873

Mots-clés

  1. 26/03/2024 26/03/2024 - Madita Rudolph
Détendeur de droits

Jorge Di Paola, MD, University of Colorado Denver Anschutz Medical Campus, Aurora, CO, USA

Téléchargé le

26 mars 2024

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000873 Exome sequencing of a family with thrombocytopenia and leukemia

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Referral to the Hemophilia and Thrombosis Center for an acute bleeding event; OR
Description

Elig.phs000873.v1.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C2585021
UMLS CUI [1,2]
C0684275
UMLS CUI [1,3]
C0040053
UMLS CUI [1,4]
C0565990
UMLS CUI [1,5]
C0019080
UMLS CUI [1,6]
C0441471
Personal or family history of bleeding; OR
Description

Elig.phs000873.v1.p1.2

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0241889
UMLS CUI [1,3]
C0019080
Personal or family diagnosis of a bleeding disorder
Description

Elig.phs000873.v1.p1.3

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0241889

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000873.v1.p1.1
Item
Referral to the Hemophilia and Thrombosis Center for an acute bleeding event; OR
boolean
C2585021 (UMLS CUI [1,1])
C0684275 (UMLS CUI [1,2])
C0040053 (UMLS CUI [1,3])
C0565990 (UMLS CUI [1,4])
C0019080 (UMLS CUI [1,5])
C0441471 (UMLS CUI [1,6])
Elig.phs000873.v1.p1.2
Item
Personal or family history of bleeding; OR
boolean
C0262926 (UMLS CUI [1,1])
C0241889 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,3])
Elig.phs000873.v1.p1.3
Item
Personal or family diagnosis of a bleeding disorder
boolean
C0005779 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0241889 (UMLS CUI [1,3])

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