Mount Sinai Hospital
Core Team
More Team Members
- Jaya Ganesh, MD
Director Newborn Screening Program
Associate Professor, Program of Inherited Metabolic Diseases
Department of Genetics and Genomic Sciences,
Icahn School of Medicine at Mount Sinai - Lissette Estrella, MS, RN, ANP, PNP
Program for Inherited Metabolic Disorders
Division of Medical Genetics
Department of Genetics and Genomic Sciences
Icahn School of Medicine - Colleen Donnelly, MS, CGC
Metabolic Genetic Counselor
Program for Inherited Metabolic Diseases
Division of Medical Genetics
Department of Genetics and Genomic Sciences
Icahn School of Medicine at Mount Sinai
Conditions Treated
Evaluate and care for patients with every form of leukodystrophy including, but not limited to:
- Krabbe disease
- Metachromatic leukodystrophy
- Adrenoleukodystrophy (ALD)
- Alexander disease
- Canavan disease
- Pelizaeus-Merzbacher disease
- Vanishing white matter disease
- Undiagnosed leukodystrophies
- Peroxisomal biogenesis disorder (PBD)
Appointments
Appointments are available urgently for patients in need of an initial evaluation or assessment.
To request an appointment or make a referral, please call Rachel Hickey, Clinic Coordinator, at (312)227-6123.
Location
Ann & Robert H. Lurie Children’s Hospital of Chicago
225 E. Chicago Avenue
Chicago, Illinois 60611
1(800)543-7362