Article
Galactose-1-phosphate uridyl transferase deficiency is not associated with Müllerian aplasia in Dutch patients.
Journal of pediatric and adolescent gynecology - 1 Aug 2009
Nijland Roel, Hartog Francis E, Wevers Ron A, Wanders Ronald J A, Willemsen Wim N P
Abstract excerpt
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 the University Medical Center Nijmegen, and compared with the general population in The Netherlands. PARTICIPANTS: Patients...
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