Neural Tube Defects Cannot Be Diagnosed Prenatally by Electrophoresis of Amniotic Fluid Transferrin Isoforms
Author(s) -
Julie Gonin,
Sophie Dreux,
Fabien Guimiot,
Françoise Ménez,
Jean Guibourdenche,
D. Biou,
Françoise Müller
Publication year - 2006
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2006.069633
Subject(s) - amniotic fluid , cerebrospinal fluid , transferrin , neural tube defect , fetus , neural tube , subarachnoid space , prenatal diagnosis , medicine , pathology , transthyretin , pregnancy , biology , embryo , genetics , microbiology and biotechnology
Prenatal diagnosis of neural tube defects (NTDs) is based on ultrasonography; but uncertainty exists in a few cases, and biochemical analysis of amniotic fluid (AF) is required. Electrophoresis of AF acetylcholinesterase is a specific and sensitive method for diagnosis of myelomeningocele (1)(2). Although false-positive results are rare, another biochemical technique would be of great value.Adult and infant cerebrospinal fluid (CSF) is characterized by a specific marker, asialotransferrin or β2-transferrin, because it migrates more slowly in electrophoresis than β1-tetrasialotransferrin, the main isoform in all biological fluids (3). The specific behavior of β2-transferrin is used for the detection of CSF leakage from the subarachnoid space into the nasal or aural cavity (4)(5). Assuming that CSF would leak from a myelomeningocele-affected fetus into the AF, we screened AF …
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