X-linked moyamoya syndrome associated with severe haemophilia A

Haemophilia. 2016 Jan;22(1):e51-4. doi: 10.1111/hae.12806. Epub 2015 Sep 30.

Authors

M Lavin^{1

2}, P V Jenkins^{1

2}, C Keenan², B White^{1

2}, D R Betts³, J S O'Donnell^{1

2}, N M O'Connell^{1

2}

Affiliations

¹ Haemostasis Research Group, Institute of Molecular Medicine, Trinity Centre for Health Sciences, St James's Hospital, Trinity College Dublin, Dublin, Ireland.
² National Centre for Hereditary Coagulation Disorders, St James's Hospital, Dublin, Ireland.
³ Department of Clinical Genetics, Our Lady's Children's Hospital, Dublin, Ireland.

PMID: 26422091
DOI: 10.1111/hae.12806

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Child
Chromosomes, Human, X / genetics*
Gene Deletion
Hemophilia A / complications*
Humans
Male
Moyamoya Disease / complications*
Moyamoya Disease / genetics*