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  2. Kallmann syndrome - Wikipedia

    en.wikipedia.org/wiki/Kallmann_syndrome

    Affected individuals with KS and other forms of HH are almost invariably born with normal sexual differentiation; i.e., they are physically male or female. This is due to the human chorionic gonadotrophin (hCG) produced by placenta at approximately 12 to 20 weeks gestation (pregnancy) which is normally unaffected by having KS or CHH. [21]

  3. Villitis of unknown etiology - Wikipedia

    en.wikipedia.org/wiki/Villitis_of_unknown_etiology

    VUE is also characterised by the transfer of maternal lymphocytes across the placenta. [2] VUE is diagnosed in 7–10% placentas in pregnancies. Roughly 80% of the VUE cases are in term placentas (greater than 37 weeks of pregnancy). A case of VUE in a placenta less than 32 weeks old should be screened for infectious villitis. [1]

  4. Placental insufficiency - Wikipedia

    en.wikipedia.org/wiki/Placental_insufficiency

    Histopathology of placenta with increased syncytial knotting of chorionic villi, with two knots pointed out. The following characteristics of placentas have been said to be associated with placental insufficiency, however all of them occur in normal healthy placentas and full term healthy births, so none of them can be used to accurately diagnose placental insufficiency: [citation needed]

  5. Intrauterine hypoxia - Wikipedia

    en.wikipedia.org/wiki/Intrauterine_hypoxia

    Intrauterine hypoxia can be attributed to maternal, placental, or fetal conditions. [12] Kingdom and Kaufmann classifies three categories for the origin of fetal hypoxia: 1) pre-placental (both mother and fetus are hypoxic), 2) utero-placental (mother is normal but placenta and fetus is hypoxic), 3) post-placental (only fetus is hypoxic).

  6. Placental disease - Wikipedia

    en.wikipedia.org/wiki/Placental_disease

    Associative prevention mechanisms can be a method of minimising the risk of developing the disease, within early stages of pregnancy. Placental syndromes include pregnancy loss, fetal growth restriction, preeclampsia, preterm delivery, premature rupture of membranes, placental abruption and intrauterine fetal demise.

  7. XY gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/XY_gonadal_dysgenesis

    XY complete gonadal dysgenesis, also known as Swyer syndrome, is a type of defect hypogonadism in a person whose karyotype is 46,XY. Though they typically have normal vulvas, [1] the person has underdeveloped gonads, fibrous tissue termed "streak gonads", and if left untreated, will not experience puberty.

  8. Placental abruption - Wikipedia

    en.wikipedia.org/wiki/Placental_abruption

    It occurs most commonly around 25 weeks of pregnancy. [2] Symptoms may include vaginal bleeding, lower abdominal pain, and dangerously low blood pressure. [1] Complications for the mother can include disseminated intravascular coagulopathy and kidney failure. [2]

  9. Pseudohermaphroditism - Wikipedia

    en.wikipedia.org/wiki/Pseudohermaphroditism

    Pseudohermaphroditism is an outdated [1] term for when an individual's gonads were mismatched with their internal reproductive system and/or external genitalia. The term was contrasted with "true hermaphroditism" (now known as ovotesticular syndrome), a condition describing an individual with both female and male reproductive gonadal tissues.

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