17-ALPHA HYDROXYPROGESTERONE, SERUM

Modification Reference values

Test code: 363

PREVIOUS Reference values

CURRENT  Reference values

Childs  (blood cord) :      9.0 -50.0  ng/mL           (Prematures) :      0.26- 5.68 ng/mL           (1 - 5 days) :      0.82- 4.20 ng/mL           (5 - 30 days):      0.1 -16.8  ng/mL           (30- 60 days):      1.9 - 9.8  ng/mL           (60- 90 days):      0.1 - 4.0  ng/mL      (Prepuberty phase):      0.10- 0.90 ng/mL      (Puberal phase)   :      0.30- 1.55 ng/mL Male                                 :  0.4 - 1.4 ng/mL Female :  Follicular phase   : 0.1 - 1.2 ng/mL                 Luteinic phase     : 0.3 - 4.8 ng/mL        Pregnant 1er Trimonthter: 0.6 -14.4 ng/mL                 2nd Trimonthter    : 2.1 -15.8 ng/mL                 3rd Trimonthter    : 3.8 -26.8 ng/mL          Oral anticonceptives  : 0.1 - 1.2 ng/mL          Menopause               : 0.1 - 0.6 ng/mL

Childs  (blood cord) :      9.0 -50.0  ng/mL           (Prematures) :      0.26- 5.68 ng/mL           (1 - 5 days) :      0.82- 4.20 ng/mL           (5 - 30 days):      0.1 -16.8  ng/mL           (30- 60 days):      1.9 - 9.8  ng/mL           (60- 90 days):      0.1 - 4.0  ng/mL      (Prepuberty phase):      0.10- 0.90 ng/mL      (Puberal phase)   :      0.30- 1.55 ng/mL Male                                 :  0.59 - 3.44 ng/mL Female :  Follicular phase   : 0.11 - 1.08 ng/mL           Luteinic phase            : 0.95 - 5.0  ng/mL        Pregnant 1er Trimonthter: 2.50 - 9.78  ng/mL                 2nd Trimonthter    : 3.40 - 8.50  ng/mL                 3rd Trimonthte     : 4.53 - 18.86 ng/mL

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ETHOSUXIMIDE (ZARONTIN), SERUM

Modification Reference values

Test code: 347

PREVIOUS Reference values	CURRENT  Reference values
Therapeutic level (childs):     40 -  80 µg/mL                                (Adults): 40 - 100 µg/mL Toxic level                        :   >  150 µg/mL	Therapeutic level (childs): 40 -  80 µg/mL                           (Adults): 40 - 100 µg/mL Toxic level                     :   >  100 µg/mL

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VITAMIN A (RETINOL), SERUM

Modification Reference values

Test code: 417

PREVIOUS Reference values	CURRENT  Reference values
From 0.2 to 0.5 mg/L	0.4 - 1.1 mg/L

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TOPIRAMATE, SERUM

Modification Method 

Test code: 3015

PREVIOUS   Method	CURRENT  Method
Fluorescente polaritation Immunoassay	Turbidimetric Immunoassay Particle

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ANTI - ALVEOLLAR-LUNGS BASEMENT MEMBRANE, SERUM

Erased test in CIC Catalog

Test Code: 2242

Discontinued for technical reason (due to the absence of reagent in the market) and decrease in demand.

ACID PHOSPHATASE- TOTAL, SERUM

Modification Reference values

Test code: 436

PREVIOUS Reference values	CURRENT  Reference values
Less than 10 U/L (37ºC)	Less than 6.5 U/L

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IRREGULAR (IDENTIFICATION AND TITRATION) ANTIBODIES, WHOLE BLOOD

Modification Sample 

Test code: 2461

PREVIOUS Sample	CURRENT  Sample
Serum	EDTA  Whole blood

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INDIRECT COOMB'S (IDENTIFICATION AND TITRATION), WHOLE BLOOD

Modification Sample 

Test code: 2230

PREVIOUS Sample	CURRENT  Sample
Serum	EDTA  Whole blood

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GUANIDINACETATE, URINE

Modification Reference values

Test code: 3288

PREVIOUS Reference values	CURRENT  Reference values
Guandinoacetate       :  9.0  - 139.0 mmol/mol creatinine creatine / creatinine :  0.01 -  1.63 mmol/mol creatinine	Guandinoacetate       creatine/creatinine  1d - 6y :         13 - 124              0.03 - 1.8 7y - 12y:          8 - 94               0.03 - 1.44 >12y    :         11 - 84               0.02 - 0.4 Units: mmol/mol creatinine

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EVEROLIMUS, TOTAL BLOOD

Modification Method 

Test code: 1503

PREVIOUS   Method	CURRENT  Method
High Performance Liquid Chromatography	Particle homogeneous immunoassay

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Kabuki, syndrome (exons 31,34,39,48 - MLL2) screening, whole blood

New Test in CIC Catalog

Test Code: 4468

Sample:	Whole blood - EDTA (5 ml)
Conservation:	Refrigerated
Method:	Sequencing Method
Set Up Days:	Daily
Delivery term:	50 days
Information:
FOR CATALOG INFORMATION SEE CODE 4467
Links:
OMIM Entry - # 147920 - KABUKI SYNDROME 1; KABUK1
Orphanet- Kabuki syndrome
OMIM Entry - - 602113 - MYELOID-LYMPHOID OR MIXED LINEAGE LEUKEMIA 2; MLL2

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Kabuki, syndrome (MLL2) sequencing, whole blood

New Test in CIC Catalog

Test Code: 4467

Sample:	Whole blood - EDTA (5 ml)
Conservation:	Refrigerated
Method:	Sequencing Method
Set Up Days:	Daily
Delivery term:	50 days
Information:
Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterized by typical facial features, skeletal anomalies, mild to moderate intellectual disability and postnatal growth deficiency. KS is associated, in 45 to 80% of cases, with mutations in the MLL2 gene. KDM6Agene deletions have also been reported in a few cases. Clinical diagnostic criteria for KS have not been established. Diagnosis relies on the clinical observation of 5 cardinal findings which are 1) cranio-facial features, 2) postnatal growth retardation, 3) skeletal anomalies, 4) persistence of fetal fingertips and 5) intellectual deficiency. Molecular analysis may confirm the clinical diagnosis. KS occurs sporadically in most cases but may have an autosomal dominant mode of inheritance with a subsequent 50% recurrence risk.
Links:
OMIM Entry - # 147920 - KABUKI SYNDROME 1; KABUK1
Orphanet- Kabuki syndrome
OMIM Entry - - 602113 - MYELOID-LYMPHOID OR MIXED LINEAGE LEUKEMIA 2; MLL2

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LOW DENSITY LIPOPROTEIN (LDL OXIDATION ) ANTIBODIES, SERUM

Modification Reference values

Test code: 1168

PREVIOUS Reference values	CURRENT  Reference values
< 0.200 D.O.	Negative:    Less than 20 EU/mL Indeterminate:    20 - 25 EU/mL Positive: Greater than 25 EU/mL

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DIAMINOXIDASE ( DAO ), PLASMA

Modification Delivery Time 

Test code: 1571

PREVIOUS Delivery Time	CURRENT  Delivery Time
Delivery time:  20 days	Delivery time: 7 days

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