Moyamoya-like cerebrovascular disease in a child with a novel mutation in myosin heavy chain 11

Neurology. 2018 Jan 16;90(3):136-138. doi: 10.1212/WNL.0000000000004828. Epub 2017 Dec 20.

Authors

Annette Keylock¹, Ying Hong¹, Dawn Saunders¹, Ebun Omoyinmi¹, Ciara Mulhern¹, Derek Roebuck¹, Paul Brogan¹, Vijeya Ganesan¹, Despina Eleftheriou²

Affiliations

¹ From UCL GOS Institute of Child Health (A.K., Y.H., E.O., C.M., P.B., V.G., D.E.); and Great Ormond Street Hospital (D.S., D.R.), London, UK.
² From UCL GOS Institute of Child Health (A.K., Y.H., E.O., C.M., P.B., V.G., D.E.); and Great Ormond Street Hospital (D.S., D.R.), London, UK. [email protected].

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Cerebrovascular Disorders / diagnostic imaging*
Cerebrovascular Disorders / genetics*
Cerebrovascular Disorders / therapy
Child, Preschool
Diagnosis, Differential
Female
Humans
Mutation*
Myosin Heavy Chains / genetics*
Phenotype

Substances

MYH11 protein, human
Myosin Heavy Chains

Grants and funding

21791/VAC_/Versus Arthritis/United Kingdom