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Dual diagnosis causing severe phenotype in a patient with Angelman syndrome

Kanani, Faraha; Mordekar, Santoshb; Parker, Michael J.a; Balasubramanian, Meenaa DDD Study

doi: 10.1097/MCD.0000000000000280
Short Case Reports

aSheffield Clinical Genetics Service

bDepartment of Paediatric Neurology, Sheffield Children’s NHS Foundation Trust, Sheffield

cWellcome Trust, Sanger Institute, Cambridge, UK

Received 6 February 2019 Accepted 25 March 2019

Correspondence to Dr Meena Balasubramanian, MBBS, DCH, FRCPCH, MD, Sheffield Clinical Genetics Service, Sheffield Children’s Hospital NHS Foundation Trust, Western Bank, Sheffield S10 2TH, UK, Tel: +44 114 2717025; fax: +44 114 2737467; e-mail:

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