The 20 Best Beckwith-Wiedemann Syndrome Doctors in The United States

Jennifer Kalish is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Kalish is rated as an Elite provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Glossectomy, and Pancreatectomy.

Arupa Ganguly is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Ganguly is rated as an Elite provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Beckwith-Wiedemann Syndrome, Macroglossia, Mosaicism, Pancreatectomy, and Tissue Biopsy.

Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Deardorff is rated as an Elite provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 29 other conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.

. Dr. Russi is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 125 other conditions, according to our data. His clinical expertise encompasses Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication. Dr. Russi is board certified in American Board Of Pediatrics and American Board Of Medical Genetics.

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 153 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, Chromosome 13q Deletion, Hennekam Syndrome, and Acrodermatitis Enteropathica.

Nina Powell is a Medical Genetics provider practicing medicine in Wilmington, Delaware. She has been practicing medicine for over 30 years. Dr. Powell is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, PIK3CA-Related Overgrowth Spectrum, Chromosome 13q Deletion, and Increased Head Circumference. Dr. Powell is board certified in American Board Of Medical Genetics And Genomics.

. Dr. Narumanchi is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Narumanchi is board certified in American Board Of Medical Genetics And Genomics.

Karen Gripp is a Medical Genetics provider practicing medicine in Wilmington, Delaware. Dr. Gripp is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 122 other conditions, according to our data. Her clinical expertise encompasses Costello Syndrome, RASopathies, Noonan Syndrome, and Gingival Fibromatosis with Hypertrichosis.

Stephanie Campbell is a Pediatrics provider practicing medicine in Royal Oak, Michigan. She has been practicing medicine for over 10 years. Dr. Campbell is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Increased Head Circumference, Delayed Growth, Congenital Athymia, and Acromesomelic Dysplasia Campailla Martinelli Type. Dr. Campbell is board certified in American Board Of Pediatrics. Dr. Campbell is currently accepting new patients.

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 Beckwith-Wiedemann 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 DiGeorge Syndrome. Dr. Grebe is board certified in Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Grebe is currently accepting new patients.

Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.

Richard Rogers is a Medical Genetics provider practicing medicine in Greenville, South Carolina. Dr. Rogers is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. His clinical expertise encompasses Macroglossia, Beckwith-Wiedemann Syndrome, and Autosomal Cleft Palate. Dr. Rogers is currently accepting new patients.

Abdallah Elias is a Medical Genetics provider practicing medicine in Salt Lake City, Utah. Dr. Elias is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses 1p36 Deletion Syndrome, Incontinentia Pigmenti, Maple Syrup Urine Disease, and Myhre Syndrome. Dr. Elias is board certified in American Board Of Medical Genetics & Genomics. Dr. Elias is currently accepting new patients.

Julie Kaplan is a Pediatrics provider practicing medicine in Cleveland, Ohio. She has been practicing medicine for over 29 years. Dr. Kaplan is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Mosaicism, Gingival Fibromatosis with Hypertrichosis, Mixed Gonadal Dysgenesis, and Turner Syndrome. Dr. Kaplan is board certified in American Board Of Medical Genetics And Genomics, 2020.

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 Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. 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.

Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Hannibal is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 166 other conditions, according to our data. His clinical expertise encompasses Aase Syndrome, CHARGE Syndrome, Cockayne Syndrome Type 2, and Hennekam Syndrome. Dr. Hannibal is board certified in Clinical Genetics & Genomics.

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 Beckwith-Wiedemann Syndrome. 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.

Laura Mackay is a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Mackay is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 132 other conditions, according to our data. Her clinical expertise encompasses Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD).

Markey Mcnutt is an Internal Medicine specialist and an Endocrinologist practicing medicine in Dallas, Texas. Dr. Mcnutt is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 122 other conditions, according to our data. His clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Phenylketonuria (PKU), and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

Ryan Gates is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Fort Worth, Texas. Dr. Gates is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Micrognathia, Von Gierke Disease, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and PIK3CA-Related Overgrowth Spectrum.