The 20 Best Miller-Dieker Syndrome Doctors Near Me in Phoenix, AZ
Find the Top Miller-Dieker Syndrome Experts and Specialists
Phoenix Children's Hospital - Genetics
Theresa Grebe is a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Grebe is rated as an Experienced provider by MediFind in the treatment of Miller-Dieker Syndrome. She is also highly rated in 96 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6 Uniparental Disomy, Temple Syndrome, Congenital Bowing of Long Bones, and Chromosome 13q Duplication. Dr. Grebe is board certified in Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Grebe is currently accepting new patients.
Phoenix Children's Hospital
Shagun Kaur is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Phoenix, Arizona. She has been practicing medicine for over 10 years. Dr. Kaur is rated as an Experienced provider by MediFind in the treatment of Miller-Dieker Syndrome. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Galactose Epimerase Deficiency, Galactosemia, and Hydranencephaly. Dr. Kaur is currently accepting new patients.
John Baker is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Baker is rated as an Experienced provider by MediFind in the treatment of Miller-Dieker Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Mosaic Variegated Aneuploidy Syndrome, Chromosome 6 Uniparental Disomy, and Tetrasomy 9p. Dr. Baker is currently accepting new patients.
Phoenix Children's Hospital
Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Knoll is rated as an Experienced provider by MediFind in the treatment of Miller-Dieker Syndrome. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Knoll is currently accepting new patients.
Last Updated: 06/30/2026
