In this section
Programs and services
- Genomic Medicine Program
- Hereditary Disorders of Connective Tissue Program
- Lysomal Storage Diseases LSD Program
- Neurofibromatosis and RASopathy Program
- Phenylketonuria PKU Program
- Undiagnosed and Rare Disease Program
- Genomic sequencing
- Request a Consult
- Undiagnosed disease process
- Undiagnosed disease team
Our team
Our team includes highly trained and experienced pediatric subspecialists, many of whom lead their field nationally. If the case requires expertise beyond those listed below, we have the advantage of being a full-service medical, surgical and diagnostic Children's Wisconsin, so the necessary resources will be brought in.
Team leader
Chief Medical Officer
- Mike Guitzeit, MD
Allergy Immunology
- Jack Routes, MD
Anesthesiology
Cardiology
Child development
Child advocacy and development
Dermatology
Endocrinology
Gastroenterology
Genetics
Hematology
Hospitalists
HMGC Center Director
- Raul Urrutia
Infectious diseases
Nephrology
Neurology
- Thomas Chelimsky, MD
- Michael Collins, MD
- Priya Monrad, MD
- Dominic Fee, MD
- Christopher Inglese
- Matt Harmelink, MD
- Amy Heffelfinger, PhD
Oncology
Ophthalmology
Pathology
Pulmonary
- Lynn D`Andrea, MD
- Louella Amos, MD
Pediatrics ethicist
Radiology
- Jack Vo, MD
- David Gregg, MD
- Tejaswini Deshmukh, MD
Research
- Mary Pat Gage
Rheumatology
Special needs
Surgery
To access our Undiagnosed and Rare Disease Program, call:
(414) 266-2771
Or fill out our online form and we'll get in touch with you.