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FLP<br />

8929<br />

FMB<br />

88841<br />

defects in the ferrochelatase gene from patients with erythropoietic protoporphyria. Am J Hum Genet<br />

1998;62:1341-1352 4. Whatley SD, Mason NG, Holme SA, et al: Molecular epidemiology of<br />

erythropoietic protoporphyria in the U.K. Br J Dermatol 2010;162:642-646<br />

Fetal Lung Profile, Amniotic Fluid<br />

Clinical Information: Respiratory distress syndrome is a common complication of prematurity<br />

occuring in infants whose lungs lack the surfactant necessary for healthy lung inflation and air exchange.<br />

Surfactant is not produced in sufficient quantity until relatively late in gestation. It is primarily made up of<br />

phospholipids such as lecithin and phosphatidylglycerol, which can be detected in amniotic fluid and used<br />

as markers for fetal lung maturity. Both the lecithin/sphingomyelin (L/S) ratio and phosphatidylglycerol<br />

(PG) concentration increase with gestational age and correlate with lung maturity. <strong>Test</strong>ing both the L/S<br />

ratio and the presence or absence of PG provides a better assessment of neonatal risk than the use of either<br />

test alone.<br />

Useful For: Determining the ability of fetal lungs to produce sufficient quantities of pulmonary<br />

surfactant Predicting the likelihood of the development of respiratory distress syndrome if the fetus were<br />

delivered<br />

Interpretation: L/S ratio or =2.5 and PG absent:<br />

indeterminate L/S ratio or =2.5 and PG trace: mature PG<br />

present: mature<br />

Reference Values:<br />

Lecithin/ Sphingomyelin Ratio Phosphatidylglycerol Interpretation<br />

Absent Immature<br />

> or =2.5 Absent Indeterminate<br />

Trace Indeterminate<br />

> or =2.5 Trace Mature<br />

Any ratio Present Mature<br />

All results will be called back.<br />

Clinical References: 1. Ashwood ER, Knight GJ: Clinical Chemistry of Pregnancy. In Tietz<br />

Textbook of Clinical Chemistry and Molecular Diagnosis, 4th Edition, Edited by Carl A Burtis, Edward R<br />

Ashwood, and David E Bruns, St Louis, MO, Elsevier Saunders, 2006, pp 2188-2192 2. Kulovich MV,<br />

Hallman MB, Gluck L: The lung profile. I. Normal pregnancy. Am J Obstet Gynecol 1979;135:57-63 3.<br />

Hill LM, Ellefson R: Variable interference of meconium in the determination of phosphatidylglycerol.<br />

Am J Obstet Gynecol 1983;147:339-340 4. Ragozzino MW, Hill LM, Breckle R, et al: The relationship of<br />

placental grade by ultrasound to markers of fetal lung maturity. Radiology 1983;148:805-807<br />

Fetomaternal Bleed, Flow Cytometry, Blood<br />

Clinical Information: In hemolytic disease of the newborn, fetal red cells become coated with IgG<br />

alloantibody of maternal origin, directed against an antigen on the fetal cells that is of paternal origin and<br />

absent on maternal cells. The IgG-coated cells undergo accelerated destruction, both before and after<br />

birth. The clinical severity of the disease can vary from intrauterine death to hematological abnormalities<br />

detected only if blood from an apparently healthy infant is subject to serologic testing. Pregnancy causes<br />

immunization when fetal red cells possessing a paternal antigen foreign to the mother enter the maternal<br />

circulation, an event described as fetomaternal hemorrhage (FMH). FMH occurs in up to 75% of<br />

pregnancies, usually during the third trimester and immediately after delivery. Delivery is the most<br />

common immunizing event, but fetal red cells can also enter the mother's circulation after amniocentesis,<br />

spontaneous or induced abortion, chorionic villus sampling, cordocentesis, or rupture of an ectopic<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 741

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