Dr Alex BroomfieldConsultant in Paediatric Inherited Metabolic Disease
Qualifications: MBBS, MSC
Registration: GMC 4342814
Professional bodies: RCPCH, BIMDG, SSIEM.
Role: Consultant in Paediatric inherited metabolic disease.
Contact: Tel 0161 701 2137 ; Fax +44 161 701 2303
Dr Alex Broomfield is a consultant in paediatric inherited metabolic diseases at the Willink Unit at Saint Mary’s Hospital.
His major research interest is therapy for lysosomal storage diseases (LSD’s) and leukodystrophys.
He received his medical training at Saint Mary’s Hospital Medical School, Imperial college, with a subsequent MSC in immunology of infectious disease at UCL. He did his metabolic training at Pedulbury Children’s Hospital and Great Ormond Street Hospital in London. Dr Broomfield has been working at the Willink Biochemical Genetics Unit in Manchester since February 2014. The Willink Unit is now part of the Manchester Centre for Genomic Medicine at Saint Mary’s Hospital.
Dr Broomfield has been actively involved in international multicentre trials of novel therapies for LSD’s. He is currently the principal or sub investigator in a number of LSD trials. He is an author of over 40 peer-reviewed papers and 1 book chapter.
When not working, he likes to travel and swim.
Clinics: General metabolic, lysosomal storage disease.