Prenatal CRH: An integrating signal of fetal distress
نویسندگان
چکیده
منابع مشابه
Pregnancy distress gets under fetal skin: Maternal ambulatory assessment & sex differences in prenatal development.
Prenatal maternal distress is associated with an at-risk developmental profile, yet there is little fetal evidence of this putative in utero process. Moreover, the biological transmission for these maternal effects remains uncertain. In a study of n = 125 pregnant adolescents (ages 14-19), ambulatory assessments of daily negative mood (anger, frustration, irritation, stress), physical activity,...
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Methods A 42-year-old gravida 2 para 1 woman was referred to our tertiary perinatology centre at 18 weeks of gestation with findings of intraabdominal calcification and anhydramnios. She did not have any complaints and her past medical history was unremarkable. This was a non-consanguineous marriage and their 10 year old child was healthy. In the current pregnancy, she did not report any use of...
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Case Report A 24-year-old primigravida was first seen for obstetric care at 13 weeks' gestation. Initially the pregnancy progressed without apparent difficulty, but the fundal height was found to be somewhat small for dates at 38 weeks' gestation. A sonogram obtained at that time showed a 33-week-sized fetus, with all measurements being concordant and no sonographic evidence of intrauterine gro...
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the umbilical vein (uv) has a non pulsating and even pattern in normal fetuses. pulsation of uv has been described in severely growth restricted fetuses with chronic hypoxia. we wanted to see whether uv pulsations could also be seen in fetuses with heart deceleration during labor, as an adjunctive measure to assess the intra partum hypoxia. in a prospective study doppler examination was perform...
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Single-Gene Disorders Invasive diagnostic prenatal (fetal) testing for molecular analysis for single-gene disorders may be considered medically necessary when a pregnancy has been identified as being at high risk: 1. For autosomal dominant conditions, at least 1 of the parents has a known pathogenic mutation. 2. For autosomal recessive conditions: a. Both parents are suspected to be carriers or...
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ژورنال
عنوان ژورنال: Development and Psychopathology
سال: 2018
ISSN: 0954-5794,1469-2198
DOI: 10.1017/s0954579418000664