Cambridge

Addenbrooke's Hospital

Address
Biochemical Genetics Unit
Addenbrooke's Hospital
Box 247
Hills Road
Cambridge
CB2 0QQ

Website: https://www.cuh.nhs.uk/our-services/pathology/

Main Contact
Ms Sarah Hogg
Director Biochemical Genetics Unit
T: 01223 596172
E: Contact Ms Sarah Hogg

Other Contacts

Mr Nick Flynn
Senior Clinical Biochemist
T: 01223 596173
E: Contact Mr Nick Flynn

Main BMS Contact
Mr Kieran McIntee
BGU Laboratory Manager
T: 01223 217160
E: Contact Mr Kieran McIntee

Dr Laura Hewitt
Senior Clinical Scientist
T: 01223596173
E: Contact Dr Laura Hewitt

LABORATORY INFORMATION


Clinical Pathology Accreditation (CPA): Yes

ISO15189: Full

UKAS No.: 9814

UKAS Website: Visit UKAS website


All | A B C G H M N O P S V
There are currently 22 names in this directory
Acyl carnitines
Dried bloodspot

Amino acids (quantitative)
Plasma [ LithiumHeparin or EDTA ] or Urine (random plain) or CSF

Biotinidase
Plasma [ LithiumHeparin ]

Chitotriosidase (Gaucher disease)
Plasma [ LithiumHeparin ]

Creatine (creatine transporter deficiency)
Plasma [ LithiumHeparin ] or Urine (frozen)

Cystine - urine (Cystinuria monitoring)
24hr collection (acid) or random

Galactose-1-phosphate uridyltransferase (Galactosaemia diagnosis)
Dried Bloodspot

Glycosaminoglycans/mucopolysaccharides (MPS screen)
Urine plain (Random)

Guanidinoacetate
Plasma [ Lithium Heparin ] or Urine Plain (random)

Homocysteine -total (Homocystinuria; CBS deficiency)
Plasma [ Lithium Heparin ]

Methylmalonate (Methylmalonic Acid)
Urine (plain random)

N-Acetylaspartate (Canavan disease)
Urine plain (random)

Organic acids (Qualitative)
Urine plain (random)

Orotic acid, orotate
Urine plain (random)

Phenylalanine/tyrosine (Phenylketonuria monitoring)
Plasma [ Lithium Heparin ] or Dried Bloodspot

Phosphoethanolamine (hypophosphatasia)
Urine plain (random)

Phytanate, phytanic acid (Peroxisomal disorders)
Plasma [ EDTA ]

Porphobilinogen (Porphyria)
Urine (Early morning urine during acute attack, protected from light and kept in plain container)

Pristanic acid, pristanate (peroxisomal disorders)
Plasma [ EDTA ]

Succinylacetone (Tyrosinaemia Type 1)
Urine plain (random)

Sulphocysteine (Sulphite oxidase deficiency; Molybdenum cofactor deficiency)
Urine plain (random)

Very long chain fatty acids
Plasma [ EDTA ]