Conditions We Treat

Our team cares for families and babies facing a wide range of genetic conditions and complications. We offer personalized support, whether you’ve already received a diagnosis or are still seeking answers. You can find help for:

• 22q11.2 deletion syndrome
• Congenital (present at birth) abdominal defects and gastrointestinal (GI) disorders
• Bone abnormalities and skeletal disorders such as:
  • Achondroplasia
  • Skeletal dysplasia 
  • Limb defects
• Cleft lip and palate
• Congenital heart disease
• Congenital neurological disorders
• Craniofacial (head and face) abnormalities
• Down syndrome (Trisomy 21)
• Edwards syndrome (Trisomy 18)
• Heterotaxy syndrome, a rare birth defect that affects the chest, heart and other organs
• Developmental and growth abnormalities
• Patau syndrome (Trisomy 13)
• Lysosomal storage diseases
• Inborn errors of metabolism, such as phenylketonuria (PKU)
• Other genetic or acquired conditions