Results 81 to 90 of about 359 (125)
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Twins with Acardia and Anencephaly
Acta geneticae medicae et gemellologiae: twin research, 1985AbstractThe authors describe a pair of twins, one of whom showed acardia while the other had severe neural tube defect including anencephaly. This is the first observation of a fetal malformation (anencephaly) in the cotwin of an acardius and confirms the fact that even the cotwin of an acardiac fetus may be at risk of severe congenital malformations.
PAVONE L +4 more
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Developmental Medicine & Child Neurology, 1973
SUMMARYThe literature on the embryology, pathology, and epidemiology of anencephaly is comprehensively reviewed. While there have been many hypotheses concerning the cause of anencephaly, none have satisfactorily explained the clinical findings, and the aetiology remains unknown.
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SUMMARYThe literature on the embryology, pathology, and epidemiology of anencephaly is comprehensively reviewed. While there have been many hypotheses concerning the cause of anencephaly, none have satisfactorily explained the clinical findings, and the aetiology remains unknown.
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Fetal hyperinsulinism in anencephaly
American Journal of Obstetrics and Gynecology, 1989Insulin was measured in the blood collected in utero from three midtrimester anencephalic fetuses. The hyperinsulinism found could be due to an underutilization of glucose in the absence of most of the brain and could be responsible for the relatively normal growth in anencephaly despite the absence of the hypothalamohypophysial axis.
Hubinont, C +3 more
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Morphologiai es igazsagugyi orvosi szemle, 1977
One case of anencephaly is described and in connection with this case factors compatible with the development of ASP are discussed. The investigation of the parent's chromosomes revealed 46, XX/47, XXX mosaicizm at the mother. The importance of genetic consultation and the intrauterin diagnosis is stressed.
B, Györgyi, O, Mária
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One case of anencephaly is described and in connection with this case factors compatible with the development of ASP are discussed. The investigation of the parent's chromosomes revealed 46, XX/47, XXX mosaicizm at the mother. The importance of genetic consultation and the intrauterin diagnosis is stressed.
B, Györgyi, O, Mária
openaire +1 more source