|Clinical Use:||The test is used to diagnose porphyrias, a group of rare disorders|
|Background:||Porphyrias are a group of rare disorders passed down through families, in which an important part of hemoglobin, heme, is not made properly. Heme is also found in myoglobin, a protein found in certain muscles. Normally, the body makes heme in a multi-step process and porphyrin’s are made during several steps of this process. Patients with porphyria have a deficiency of certain enzymes required for this process. This causes abnormal amounts of porphyrins or related chemicals to build up in the body. There are many different forms of porphyria. The most common type is porphyria cutanea tarda (PCT). Drugs, infection, alcohol, and hormones such as estrogen may trigger attacks of certain types of porphyria. Porphyrias involve three major symptoms:
Attacks can occur suddenly, usually with severe abdominal pain followed by vomiting and constipation. Being out in the sun can cause pain, sensations of heat, blistering, and skin redness and swelling. Urine may turn red or brown after an attack. Other symptoms may include: muscle pain, muscle weakness or paralysis, numbness or tingling, pain in the arms or legs, pain in the back & personality changes.
|Specimen Requirements:||Heparin or EDTA tube. Centrifuge, remove plasma, and add an approx. equal volume of saline to the cell pellet. Mix and re-centrifuge. Remove and discard ALL supernatant. Transfer 1.0 mL packed cells to plastic LIP tube.Specimen type to be referred depends upon relevant clinical symptoms of the patient. If in doubt consult with Clinical Biochemist or Senior BMS.
ALL SPECIMENS SHOULD BE PROTECTED FROM LIGHT DURING COLLECTION, TRANSPORT TO LAB AND SUBSEQUENT STORAGE.
|Turnaround Time:||4 weeks|
|Additional Information:||The following supporting information should be included on request forms.
|Referred Test:||Referred test|
|Location:||King’s College Hospital|