The 20 Best Carnitine Palmitoyltransferase 2 Deficiency Doctors in The United States

Mark Skier is a primary care provider, practicing in Internal Medicine in Milwaukee, Wisconsin. Dr. Skier is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. His clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Ulcerative Colitis, and Glucocorticoid-Remediable Aldosteronism. Dr. Skier is board certified in American Board Of Internal Medicine.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 8 years. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics, American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics.

. Dr. Arnold is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Mitochondrial Trifunctional Protein Deficiency, Krabbe Disease, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. Arnold is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.

Hunter Underhill is a Medical Genetics provider practicing medicine in Salt Lake City, Utah. Dr. Underhill is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Carnitine Palmitoyltransferase 1 Deficiency, Carnitine Palmitoyltransferase 2 Deficiency, DPAGT1-CDG, and Fabry Disease. Dr. Underhill is board certified in American Board Of Pediatrics. Dr. Underhill is currently accepting new patients.

Beth Kaufman is a Pediatric Cardiologist practicing medicine in Palo Alto, California. Dr. Kaufman is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Duchenne Muscular Dystrophy, Cardiomyopathy, Dilated Cardiomyopathy (DCM), Becker Muscular Dystrophy, and Heart Transplant.

Linda Rossetti is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 10 years. Dr. Rossetti is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 87 other conditions, according to our data. Her clinical expertise encompasses Smith-Magenis Syndrome, Miller-Dieker Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Rossetti is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Anum Saeed is a Cardiologist practicing medicine in Pittsburgh, Pennsylvania. Dr. Saeed is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Atherosclerosis, High Cholesterol, Carnitine Palmitoyltransferase 2 Deficiency, Familial Hypertriglyceridemia, and Heart Bypass Surgery. Dr. Saeed is board certified in American Board Of Internal Medicine and American Board Of Internal Medicine.

I specialize in brain development and treat children with brain disorders. I have a particular interest in children with prenatal brain malformations, perinatal brain injury, cerebral palsy, and genetic and developmental brain disorders. It is incredibly scary for any family to be worried about their child's brain. My goal is to provide thoughtful, honest, compassionate care to guide families towards a realistic but hopeful understanding of their child's condition and available treatment options. Since I see patients at the beginning of their life's journey, my hope is that they will maximize their unique developmental potential. I aim to provide the support and resources at my disposal to help them do so. Dr. Russ is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. His clinical expertise encompasses Agyria Pachygyria Polymicrogyria, Carnitine Palmitoyltransferase 2 Deficiency, Anencephaly, and Asphyxia Neonatorum. Dr. Russ is board certified in American Board Of Psychiatry/Neurology, Neurology With Special Qualifications In Child Neurology.

Dr. DiBartolomeo specializes in neonatology in the Johns Hopkins All Children’s Maternal, Fetal & Neonatal Institute. Dr. DiBartolomeo earned her medical degree from Nova Southeastern University in Fort Lauderdale, Florida. She trained in pediatrics and completed a neonatology fellowship at University of Chicago, Comer Children’s Hospital. While at the University of Chicago, Dr. DiBartolomeo concurrently completed a clinical medical ethics fellowship through the MacLean Center for Clinical Medical Ethics. Additionally, she holds a Master of Public Health from Nova Southeastern University. At Johns Hopkins All Children’s Hospital, Dr. DiBartolomeo is the physician chair for the Human Values and Ethics Committee and serves on the Medical Executive Committee. She worked to develop and launch the Johns Hopkins All Children’s Fetal Care Program and serves as the medical director of the program, working with maternal-fetal medicine colleagues as well as various pediatric subspecialists to provide prenatal consultation and counseling, and to offer a coordinated, family-centered approach to the diagnosis and treatment of fetal anomalies that brings perinatal, neonatal and pediatric specialists to the patient. Her clinical and research interests include perinatal care and counseling, clinical medical ethics, neonatal palliative care and ethical issues at the margins of viability. Dr. Dibartolomeo is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. Her clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Infantile Apnea, Aplasia Cutis Congenita, and Ectodermal Dysplasias. Dr. Dibartolomeo is board certified in American Board Of Pediatrics.

Aykut Tugertimur is a Pediatric Cardiologist practicing medicine in New Hyde Park, New York. Dr. Tugertimur is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Kawasaki Disease, Cor Triatriatum, Patent Ductus Arteriosus, and Ventricular Septal Defects. Dr. Tugertimur is board certified in American Board Of Pediatrics/Pediatric Cardiology.

Raymond Wang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Wang is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 50 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

Nicki Cain is a Pediatrics provider practicing medicine in Caledonia, Michigan. She has been practicing medicine for over 18 years. Dr. Cain is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Obesity in Children, Croup, Herpangina, and Carnitine Palmitoyltransferase 2 Deficiency. Dr. Cain is board certified in American Board Of Pediatrics. Dr. Cain is currently accepting new patients.

Melissa Wasserstein is a Pediatrics provider practicing medicine in Bronx, New York. Dr. Wasserstein is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Reticulohistiocytoma, and Splenomegaly.

Dr. Michael Leahy, MD is a board certified orthopedic surgeon in The Woodlands, TX and has been practicing for 21 years. He specializes in orthopedic surgery. He received his medical degree from University of Texas Medical Branch and has been in practice between 11-20 years. Dr. Leahy is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Spinal Stenosis, Spondylolisthesis, Herniated Disk, Herniated Disc Surgery, and Cervical Disc Surgery. Dr. Leahy is currently accepting new patients.

Laura Mariani is an Internal Medicine specialist and a Nephrologist practicing medicine in Ann Arbor, Michigan. Dr. Mariani is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Minimal Change Disease, Glomerulonephritis, Carnitine Palmitoyltransferase 2 Deficiency, and Thin Basement Membrane Nephropathy.

Dr. Pritchard is a Michigan native who returned to the University of Michigan to join the faculty here in 2019 after completing her pediatrics and genetics residencies and biochemical genetics fellowship. She enjoys care of complex patients with rare genetic diseases. Dr. Pritchard is active in medical education as Program Director for the Medical Biochemical Genetics Fellowship program and Associate Program Director for the Medical Genetics and Genomics training programs.Outside of work, Dr. Pritchard enjoys cooking, reading, hiking, and spending time with her husband and two daughters. Dr. Pritchard is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 149 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Cohen Syndrome.

Dr. DiMagno grew up in southern Illinois and completed her undergraduate studies in Biology at Washington University in St. Louis. She earned her medical degree from the University of Illinois at Chicago and completed her Internal Medicine residency at the University of Michigan in 1998. She is board certified in Internal Medicine.She joined the faculty at Michigan Medicine in 1998 and spent 20 years practicing Primary Care General Internal Medicine at the Brighton Health Center. In 2018, she became part of the founding team of the newly opened Victors Care program, where she continues to provide personalized, relationship-based care. She was appointed Medical Director in 2021.Her clinical interests include patient-physician communication, preventive care, women’s health, and behavior change in chronic disease. A longtime educator of medical students and residents, Dr. DiMagno brings that experience into her practice through clear communication and shared decision-making. She emphasizes personalized, evidence-informed care grounded in trust, continuity, and a desire to understand each patient’s values and goals.She and her husband, Matthew, have four children, now ranging from middle school through college. Much of her free time is spent cheering them on from the sidelines of hockey, soccer, and lacrosse—hockey remains her favorite. She has played recreational hockey since her daughter first took up the sport and continues to enjoy the game. She also enjoys supporting her children’s musical performances and spending time outdoors and with family. Dr. Dimagno is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Bloom Syndrome, and Urticaria Pigmentosa. Dr. Dimagno is board certified in Internal Medicine.

Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.

Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Scheuerle is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. She is also highly rated in 170 other conditions, according to our data. Her clinical expertise encompasses Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.