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Immunodeficiency – centromeric instability – facial dysmorphism (ICF) syndrome: evaluation of characteristics and outcome after allogeneic haematopoietic stem cell transplantation

Inborn Errors Working Party (IEWP)
Study number:
Short title:
ICF syndrome
Primary objective:
Key inclusion criteria:
ICF syndrome patients (all ages; genetically confirmed or strong clinical suspicion) that have undergone HSCT.
Principal investigator:
Dagmar Berghuis
EBMT Study coordinator:
Sheree Hazelaar/ Jorinde Hoogenboom
Study coordinator email: