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  2. Polyhydramnios - Wikipedia

    en.wikipedia.org/wiki/Polyhydramnios

    Polyhydramnios is a medical condition describing an excess of amniotic fluid in the amniotic sac.It is seen in about 1% of pregnancies. [1] [2] [3] It is typically diagnosed when the amniotic fluid index (AFI) is greater than 24 cm. [4] [5] There are two clinical varieties of polyhydramnios: chronic polyhydramnios where excess amniotic fluid accumulates gradually, and acute polyhydramnios ...

  3. Kagami-Ogata Syndrome - Wikipedia

    en.wikipedia.org/wiki/Kagami-Ogata_Syndrome

    Kagami-Ogata syndrome is a rare genetic disease that is caused by mutations on Maternal chromosome 14 or by paternal UPD(14). [1] The main signs of this disease are: polyhydramnios , narrow bell-shaped thorax , coat-hanger-like ribs , abdominal wall defect , enlarged placenta . [ 2 ]

  4. PHACE syndrome - Wikipedia

    en.wikipedia.org/wiki/PHACE_syndrome

    PHACE syndrome is a medical condition characterized by uncommon associations between birth defects of the brain, skin (large facial infantile hemangiomas), arteries, heart and eyes. "PHACE" is an acronym for the parts of the body the syndrome usually impacts: Posterior fossa abnormalities and other structural brain abnormalities.

  5. Blepharophimosis, ptosis, epicanthus inversus syndrome

    en.wikipedia.org/wiki/Blepharophimosis,_ptosis...

    Other common symptoms include lack of an eyelid fold, an appearance of widely spaced eyes (telecanthus), low nose bridge and ear malformations (including cupping and incomplete development). Rare symptoms include microphthalmos (abnormally small eyes), tear ducts in the wrong location and a high-arched palate . [ 1 ]

  6. Perlman syndrome - Wikipedia

    en.wikipedia.org/wiki/Perlman_syndrome

    Perlman syndrome (PS), also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, is a rare overgrowth syndrome caused by autosomal recessive mutations in the DIS3L2 gene. PS is characterized by macrocephaly , neonatal macrosomia , nephromegaly , renal dysplasia, dysmorphic facial features, and increased risk for Wilms ...

  7. Mirror syndrome - Wikipedia

    en.wikipedia.org/wiki/Mirror_syndrome

    Mirror syndrome, triple edema or Ballantyne syndrome is a rare disorder affecting pregnant women. It describes the unusual association of fetal and placental hydrops with maternal preeclampsia. [1] The name "mirror syndrome" refers to the similarity between maternal edema and fetal hydrops. It was first described in 1892 by John William ...

  8. Sacrococcygeal teratoma - Wikipedia

    en.wikipedia.org/wiki/Sacrococcygeal_teratoma

    Else if SCT over 5–10 cm or polyhydramnios, perform early (37 weeks gestation) elective Cesarean section; Else SCT small and no complications, permit term spontaneous vaginal delivery; Emergent problems include maternal mirror syndrome, polyhydramnios, and preterm labor. Poor management decisions, including interventions that are either ...

  9. Adie syndrome - Wikipedia

    en.wikipedia.org/wiki/Adie_syndrome

    Adie syndrome, also known as Holmes–Adie syndrome, is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodation (i.e., light-near dissociation). [1] It is frequently seen in females with absent knee or ankle jerks and impaired sweating.