Fetal Treatment Program of New England
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Polycystic Kidney Disease
Polycystic kidney disease is an inherited disease in which cysts develop on both kidneys after birth. The age of onset and severity depend on the specific genetic pattern in the family. Diagnosed through routine prenatal ultrasound, computed tomography, nuclear scanning and fetal MRI, polycystic kidney disease can only be treated after birth with dialysis or kidney transplant.
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
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