Fetal Treatment Program of New England
Fetal Treatment Program of New England
- Who We Are
- Why Choose Us
- Our Services
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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
- Meet Our Team
- Research
- Success Stories
- Licensure, Accreditations and Memberships
- Resources
- Contact Us
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Micrognathism and Pierre Robin Sequence
Seen in approximately one in 8,500 live births, micrognathia and Pierre Robin sequence are related conditions in which the jaw or chin is smaller than normal, causing breathing and feeding problems at birth. Diagnosed through level II ultrasound, fetal MRI, echocardiogram and amniocentesis, these conditions cannot be treated with fetal intervention and may require surgery at birth.
