Fetal Treatment Program of New England
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Esophageal Atresia
Seen in approximately one in 4,000 births and caused by the abnormal development of the esophagus, esophageal atresia refers to the incomplete connection of the mouth to the stomach, which causes swallowing and breathing problems at birth. Diagnosed through level II ultrasound, fetal echocardiogram and amniocentesis, esophageal atresia is best treated after birth with surgery; however, more than one procedure may be needed to repair the connection. Your baby will remain in the hospital for several weeks while normal swallowing function is restored, and will receive nutrients intravenously until he or she can consume enough nutrients for normal growth through mouth feedings.
Fetal Treatment Program of New England
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Conditions We Treat
- Abdominal Cysts
- Amniotic Band Syndrome
- Bladder Exstrophy
- Cleft Lip and Palate
- Club Foot
- Congenital Diaphragmatic Hernia (CDH)
- Congenital Heart Disease
- Congenital High Airway Obstruction Syndrome (CHAOS)
- Congenital Lung Lesions
- Congenital Tumors
- Congenital Urinary Tract Obstruction
- Craniosynostosis
- Duodenal Atresia
- Esophageal Atresia
- Fetal Arrhythmia/Dysrhythmia
- Gastroschisis
- Hydrocephalus
- Hypoplastic Left and Right Heart Syndrome
- Intestinal Atresia
- Lymphatic and Vascular Malformations
- Micrognathism and Pierre Robin Sequence
- Multicystic Dysplastic Kidney Disease
- Omphalocele
- Ovarian Cysts
- Polycystic Kidney Disease
- Twin-to-Twin Transfusion Syndrome
- Prune Belly Syndrome
- Spina Bifida
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