MediFind found 5 doctor with experience in Chromosome 2 Uniparental Disomy near Grand Rapids, MI. Of these, 5 are Experienced.
Spectrum Health Hospitals
Linda Rossetti is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Rossetti has been practicing medicine for over 9 years and is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. Her top areas of expertise are Miller-Dieker Syndrome, Smith-Magenis Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Rossetti is currently accepting new patients.
Spectrum Health Primary Care Partners
Steven Deroos is a Pediatric Neurologist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Deroos is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. His top areas of expertise are Cerebral Palsy, Spastic Diplegia Infantile Type, Moebius Syndrome, and Dandy-Walker Syndrome. Dr. Deroos is currently accepting new patients.
Timothy Moss is a Medical Genetics provider in Grand Rapids, Michigan. Dr. Moss is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. His top areas of expertise are Proteus-Like Syndrome, Proteus Syndrome, Weaver Syndrome, and Simpson-Golabi-Behmel Syndrome.
Spectrum Health Primary Care Partners
Paul Twydell is a Neurologist in Grand Rapids, Michigan. Dr. Twydell is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. His top areas of expertise are Myasthenia Gravis, Monomelic Amyotrophy, Chronic Inflammatory Demyelinating Polyneuropathy, and Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease). Dr. Twydell is currently accepting new patients.
Spectrum Health Primary Care Partners
Jessica Priestley is a Medical Genetics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Priestley is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is currently accepting new patients.
Last Updated: 10/30/2025