A prospective study of pediatric hereditary hematological disorders

A prospective study of pediatric hereditary hematological disorders - A prospective study of pediatric hereditary hematological disorders

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000037774

Enrollment

1000

Registered

2019-09-01

Start date

2019-09-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric hereditary hematological disorders

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients under 40 years old who are diagnosed or suspected with disease below; Fanconi anemia, Diamond-Blackfan anemia, Dyskeratosis congenita, Congenital sideroblastic anemia, Severe congenital neutropenia, Congenital dyserythropoietic anemia, Congenital amegakaryocyte thrombocytopenia, Congenital thrombocytopenia, Congenital hemolytic anemia, unclassified inherited hematological disorders, primary immunodeficiencies

Exclusion criteria

Exclusion criteria: Patients who don't meet the inclusion criteria

Design outcomes

Primary

Measure	Time frame
The number of patients enrolled in this research.	—

Countries

Japan,Asia(except Japan),North America,South America,Australia,Europe,Africa

Contacts

Public ContactHideki Muramatsu

Nagoya university graduate school of medicine Department of pediatrics

hideki-muramatsu@med.nagoya-u.ac.jp+81-52-744-2294

Outcome results