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  2. List of fetal abnormalities - Wikipedia

    en.wikipedia.org/wiki/List_of_fetal_abnormalities

    Fetal abnormalities are conditions that affect a fetus or embryo, are able to be diagnosed prenatally, and may be fatal or cause disease after birth. They may include aneuploidies, structural abnormalities, or neoplasms. Acardiac twin; Achondrogenesis; Achondroplasia

  3. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    A congenital malformation is a physical anomaly that is deleterious, i.e. a structural defect perceived as a problem. A typical combination of malformations affecting more than one body part is referred to as a malformation syndrome. [citation needed] Some conditions are due to abnormal tissue development:

  4. Intestinal malrotation - Wikipedia

    en.wikipedia.org/wiki/Intestinal_malrotation

    Intestinal malrotation is a congenital anomaly of rotation of the midgut. It occurs during the first trimester as the fetal gut undergoes a complex series of growth and development. Malrotation can lead to a dangerous complication called volvulus, in which cases emergency surgery is indicated. [1]

  5. Congenital vertebral anomaly - Wikipedia

    en.wikipedia.org/wiki/Congenital_vertebral_anomaly

    Congenital vertebral anomalies are a collection of malformations of the spine. Most, around 85%, are not clinically significant, but they can cause compression of the spinal cord by deforming the vertebral canal or causing instability. This condition occurs in the womb.

  6. VACTERL association - Wikipedia

    en.wikipedia.org/wiki/VACTERL_association

    A - Anorectal malformations; C - Cardiovascular anomalies; T - Tracheoesophageal fistula; E - Esophageal atresia; R - Renal (Kidney) and/or radial anomalies; L - Limb defects; Although it was not conclusive whether VACTERL should be defined by at least two or three component defects, [4] it is typically defined by the presence of at least three ...

  7. Fetal warfarin syndrome - Wikipedia

    en.wikipedia.org/wiki/Fetal_warfarin_syndrome

    Fetal warfarin syndrome is a disorder of the embryo which occurs in a child whose mother took the medication warfarin (brand name: Coumadin) during pregnancy. Resulting abnormalities include low birth weight , slower growth , intellectual disability , deafness , small head size , and malformed bones , cartilage , and joints .

  8. Abdominal wall defect - Wikipedia

    en.wikipedia.org/wiki/Abdominal_wall_defect

    Abdominal wall defects are a type of congenital defect that allows the stomach, the intestines, or other organs to protrude through an unusual opening that forms on the abdomen. [ 1 ] [ 2 ] During the development of the fetus, many unexpected changes occur inside the womb.

  9. Frontonasal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Frontonasal_dysplasia

    Frontonasal dysplasia (FND) is a congenital malformation of the midface. [1] For the diagnosis of FND, a patient should present at least two of the following characteristics: hypertelorism (an increased distance between the eyes), a wide nasal root, vertical midline cleft of the nose and/or upper lip, cleft of the wings of the nose, malformed nasal tip, encephalocele (an opening of the skull ...