In most cases, the exact cause cannot be identified. Amniotic fluid is created from fetal urine, and is decreased by fetal swallowing and absorption in their gut. In another study, all patients with polyhydramnios, that had a sonographically normal fetus, showed no chromosomal anomalies. Molecular diagnosis is available for these conditions. • Neurological abnormalities such as
anencephaly, which impair the swallowing reflex. Anencephaly is failure of closure of the rostral neuropore (rostral neural tube defect). If the rostral neuropore fails to close there will be no neural mechanism for swallowing. • Chromosomal abnormalities such as
Down syndrome and
Edwards syndrome, which is itself often associated with gastrointestinal abnormalities. • Skeletal dysplasia, or dwarfism. There is a possibility of the chest cavity not being large enough to house all of the baby's organs causing the trachea and esophagus to be restricted, not allowing the baby to swallow the appropriate amount of amniotic fluid. • Sacrococcygeal
teratoma ==Diagnosis==