Adenosine Deaminase (ADA)
Disease
ADA deficiency.
Description
Adenosine deaminase (ADA) catalyzes the deamination of adenosine to inosine and a deficiency leads to a form of severe combined immunodeficiency (SCID). Elevated ADA activity is associated with Blackfan Diamond Anemia.
OMIM
Method
HPLC-UV
Price
€ 472
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Blood spots.
- Conditions: room temperature.
- Specifics: At least 4.5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Blood spots
- Conditions: Room temperature.
- Specifics: 4 blood spots are prepared on Guthrie cards with 40 µl EDTA-anticoagulated blood per spot. The Guthrie card is to be air-dried at room temperature for 4 hours. The Guthrie card has to be clearly labeled (with name of patient and date of birth) and should arrive at our laboratory at room temperature within 3 days.
- TAT: 3 weeks.
Dihydropyrimidine dehydrogenase (DPD)
Disease
DPD deficiency.
Description
Catalyzes the first reaction of the pyrimidine degradation pathway. A deficiency is associated with neurological abnormalities and severe 5FU toxicity.
OMIM
Method
LC-MS/MS
Price
€ 722
Test request form Enzyme diagnostics
Attention:
Samples should arrive Monday through Thursday from 8:30 AM to 4:00 PM and Friday or the day prior to a national holiday before 12:00 AM (GMT+1.00). Our laboratory is closed on the national holidays, see Shipment & Contact
Materials:
Whole EDTA blood
- Test material: peripheral blood mononuclear cells isolated from whole blood.
- Conditions: room temperature.
- Specifics: At least 15 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 36 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 2 weeks.
Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)
Disease
Lesch-Nyhan syndrome or HGPRT deficiency.
Description
Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) has a central role in the generation of purine nucleotides through the purine salvage pathway. HGPRT (EC 2.4.2.8), catalyzes the conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. A deficiency is associated with Lesch-Nyhan disease (OMIM 300322).
OMIM
Method
HPLC-UV
Price
€ 472
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Erythrocytes isolated from whole blood.
- Conditions: room temperature.
- Specifics: 2-5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Erythrocytes
- Test material: Erythrocytes.
- Conditions: Dry ice.
- Specifics: 200 µl packed erythrocytes from EDTA blood of the patient should be sent in clearly labeled (with name of patient and date of birth), tightly capped tubes, stored at -80 °C and subsequently shipped on dry ice. Do not use PBS for preparation of packed erytrocytes but use 0.9% NaCl. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Phosphoribosylpyrophosphate synthetase (PRPPs)
Disease
PRPP synthetase deficiency or superactivity.
Description
Phosphoribosylpyrophosphate synthetase (PRPPs) is the first enzyme of the purine de novo pathway and a superactivity leads to gout. A deficiency is associated with Charcot-Marie-Tooth Disease and Arts syndrome.
OMIM
Method
HPLC-UV
Price
€ 472
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Erythrocytes isolated from whole blood.
- Conditions: room temperature.
- Specifics: 2-5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Erythrocytes
- Test material: Erythrocytes.
- Conditions: Dry ice.
- Specifics: 200 µl packed erythrocytes from EDTA blood of the patient should be sent in clearly labeled (with name of patient and date of birth), tightly capped tubes, stored at -80 °C and subsequently shipped on dry ice. Do not use PBS for preparation of packed erytrocytes but, use 0.9% NaCl. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Purine Nucleoside Phosphorylase (PNP)
Disease
PNP deficiency.
Description
Purine nucleoside phosphorylase (PNP) is an essential enzyme of the purine degradation pathway and patients with PNP deficiency are diagnosed by severe T-cell immunodysfunction, hypouricemia.
OMIM
Method
HPLC-UV
Price
€ 472
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Blood spots.
- Conditions: room temperature.
- Specifics: At least 4.5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Blood spots
- Conditions: Room temperature.
- Specifics: 4 blood spots are prepared on Guthrie cards with 40 µl EDTA-anticoagulated blood per spot. The Guthrie card is to be air-dried at room temperature for 4 hours. The Guthrie card has to be clearly labeled (with name of patient and date of birth) and should arrive at our laboratory at room temperature within 3 days.
- TAT: 3 weeks.
Thiopurine methyltransferase (TPMT)
Disease
TPMT deficiency.
Description
Thiopurine methyltransferase (TPMT) catalyzes the methylation of 6-mercaptopurine.
OMIM
Method
HPLC-UV
Price
€ 472
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Erythrocytes isolated from whole blood.
- Conditions: room temperature.
- Specifics: 2-5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Erythrocytes
- Test material: Erythrocytes.
- Conditions: Dry ice.
- Specifics: 200 µl packed erythrocytes from EDTA blood of the patient should be sent in clearly labeled (with name of patient and date of birth), tightly capped tubes, stored at -80 °C and subsequently shipped on dry ice. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Thymidine phosphorlylase (TP)
Disease
MNGIE.
Description
Thymidine phosphorylase (TP) catalyzes the degradation of thymidine and a deficiency is associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
OMIM
Price
€ 472
Method
HPLC-UV
Test request form Enzyme diagnostics
Materials:
Whole EDTA blood
- Test material: Blood spots / leukocytes.
- Conditions: room temperature.
- Specifics: 2-5 ml EDTA blood of the patient should be sent AT ROOM TEMPERATURE in clearly labeled (with name of patient and date of birth), tightly capped tubes, wrapped in protective material, placed in a sealed plastic bag and shipped by courier service in a Styrofoam shipping box. Blood samples need to arrive in our laboratory within 48 hours after drawing. Include one blood sample as a control for shipment conditions. Please complete the test request form and send it along with the sample.
- TAT: 3 weeks.
Blood spots
- Conditions: Room temperature.
- Specifics: 4 blood spots are prepared on Guthrie cards with 40 µl EDTA-anticoagulated blood per spot. The Guthrie card is to be air-dried at room temperature for 4 hours. The Guthrie card has to be clearly labeled (with name of patient and date of birth) and should arrive at our laboratory at room temperature within 3 days.
- TAT: 3 weeks.