Fetal Care Services
Offering hope to families of infants with congenital differences.
The Fetal Care Service team offers support to families expecting an infant with medical needs that require intervention at birth. We provide comprehensive, coordinated care from prenatal diagnosis to the transition to infant care.
Learning your unborn baby will be born with a medical condition can be devastating. Families are faced with uncertainty and an endless list of questions about the future of the unborn baby.
Our Fetal Care navigators at Nicklaus Children's are devoted to the care of infants pre-diagnosed with medical needs in utero that will require intervention at birth.
The team well understands the concerns of families anticipating an infant with a complex diagnosis. The Nicklaus Children's network of pediatric subspecialists collaborate with prenatal care providers in the community and beyond to provide families comprehensive, coordinated care and support from prenatal testing to the transition to infant care.
Initial Consultation and Scheduling
Our Fetal Care nurse navigators are committed to optimizing care access and convenience for expectant families. The navigator is the first contact for families to discuss issues and concerns. The navigator arranges the appointments for all diagnostic tests and specialty consultations with the family. The goal is to support families in obtaining a definitive plan of care, definitive diagnosis and counseling plan during a single visit, when possible. The appointment may include:
- Diagnostic tests
- Prenatal counseling
- Genetic consultation
- Diagnosis-specific subspecialty consultations
Specialist Programs and Services
Conditions we Treat
- Abdominal Wall Abnormalities
- Beckwith-Wiedemann Syndrome
- Birth Defects and Congenital Anomalies
- Cleft Lip and/or Palate
- CLOVES Syndrome
- Clubfoot
- Congenital Diaphragmatic Hernia
- Congenital Hand Malformation
- Congenital Heart Defects/Disease
- Congenital High Airway Obstruction Syndrome
- Congenital Limb Differences
- Congenital Pulmonary Airway Malformation (CPAM)
- Craniofacial Abnormalities
- Craniofacial Microsomia
- Craniosynostosis
- Down Syndrome
- Encephalocele
- Gastroschisis and Omphalocele
- Genetic Diseases
- Hemolytic Disease
- Hydrocephalus
- Hydronephrosis
- Hyperbilirubinemia and jaundice
- Hypoplastic Left Heart Syndrome (HLHS)
- Inborn Errors of Metabolism
- Intestinal Atresia, and Stenosis and Intestinal Cysts
- Macroglossia
- Mediastinal Teratoma
- Multicystic Dysplastic Kidney
- Myelomeningocele
- Neural Tube Defects
- Neurogenetic–Neurometabolic Abnormalities
- Periventricular Leukomalacia
- Pierre Robin Sequence
- Sacrococcygeal Teratoma
- Single Ventricle Heart Defects (SVD)
- Spina Bifida
- Tetralogy of Fallot
- Transposition of the Great Arteries
- Treacher Collins Syndrome
- Ureterocele
- Vitamin K deficiency bleeding
Prenatal Diagnostic Tests



