Galactose-1-Phosphate Uridyl Transferase Deficiency Is Not Associated with Müllerian Aplasia in Dutch Patients

Abstract Study Objective To study whether a deficiency in galactose-1-phosphate uridyl transferase (GALT) activity of mothers was an explanation for the occurrence of Müllerian aplasia of their daughters. Design A case control study. Setting The patients were selected from the outpatient clinic of t...

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Veröffentlicht in:	Journal of pediatric & adolescent gynecology 2009-08, Vol.22 (4), p.229-231
Hauptverfasser:	Nijland, Roel, MD, PhD, Hartog, Francis E., MD, Wevers, Ron A., PhD, Wanders, Ronald J.A., PhD, Willemsen, Wim N.P., MD, PhD
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Case-Control Studies Female Galactose - urine Galactose-1-phosphate uridyl transferase Humans Middle Aged MRKH Mullerian Ducts - abnormalities Müllerian aplasia Netherlands Obstetrics and Gynecology Pediatrics Polymorphism, Single Nucleotide Pregnancy Syndrome UTP-Hexose-1-Phosphate Uridylyltransferase - genetics Young Adult
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