The 20 Best Branchio-Oculo-Facial Syndrome (BOFS) Doctors in The United States

Guney Bademci is a Medical Genetics provider practicing medicine in Miami, Florida. Dr. Bademci is rated as an Elite provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Branchiootorenal Syndrome, Branchio-Oculo-Facial Syndrome (BOFS), Oculofaciocardiodental Syndrome, and KBG Syndrome. Dr. Bademci is currently accepting new patients.

Jeff Milunsky is a Medical Genetics provider practicing medicine in Cambridge, Massachusetts. Dr. Milunsky is rated as a Distinguished provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Branchio-Oculo-Facial Syndrome (BOFS), Branchiootorenal Syndrome, Micrognathia, and Coffin-Siris Syndrome. Dr. Milunsky is currently accepting new patients.

Ingrid Holm is a Pediatric Endocrinologist practicing medicine in Boston, Massachusetts. Dr. Holm is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 13 other conditions, according to our data. Her clinical expertise encompasses Sudden Infant Death Syndrome (SIDS), Brachydactyly Mononen Type, Renpenning Syndrome, and FG Syndrome.

Dr. Couser obtained his bachelor’s degree from the University of Virginia and his Medical Doctorate from the Virginia Commonwealth University School of Medicine (VCU SOM). Dr. Couser’s ophthalmology residency was completed at Howard University where he served as co-chief resident in the last year of his residency. He received fellowship training in pediatric ophthalmology and adult strabismus at Emory University. Dr. Couser received a master’s degree in biotechnology from the Johns Hopkins University and completed a residency in clinical genetics at the University of North Carolina at Chapel Hill. He is one of only a few individuals currently board-certified by both the American Board of Ophthalmology and the American Board of Medical Genetics and Genomics. CV https://www.hopkinsmedicine.org/-/media/wilmer/documents/cvs/couser-cv Research Summary My primary research focus involves the identification and management of genetic eye diseases including rare inherited disorders affecting the eyes. Research and scholarly activities have been an integral component of my career path. I have been the principal investigator on 10 clinical trial/IRB studies and a co-investigator on others, participated with several committees or advisory panels related to research activities. I have been credited with over 120 book chapter, journal article and abstract publications. In addition, I served as the primary author/sole editor for a textbook titled Ophthalmic Genetic Diseases: A Quick Reference Guide to the Eye and External Ocular Adnexa Abnormalities, 1st Edition, published by Elsevier in 2018, which is one of only a few textbooks published in this subject area. I also served as a grant review panelist for the National Eye Institute Career Development Awards. Selected Publications *Couser NL, Masood MM, Strande NT, Foreman AKM, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM. 2015. The phenotype of multiple congenital anomalies- hypotonia-seizures syndrome 1: Report and review. Am J Med Genet Part A 9999A:1–6 *Couser NL, Lambert SR. Botulinum toxin: A treatment of consecutive esotropia in children. Strabismus 2012; 20(4):158-161 Couser NL, Lenhart PD, Hutchinson AK. Augmented Hummelsheim procedure to treat complete abducens nerve palsy. J AAPOS 2012;16(4):331-5 *Natario L. Couser, Maheer M. Masood, Arthur S. Aylsworth, and Roger E. Stevenson. Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic Genet. 2017, Jan 23:1-12 *Couser NL, Brooks BP, Drack AV, Shankar SP. The evolving role of genetics in ophthalmology. Ophthalmic Genet. 2021 Jan 12:1-4. doi: 10.1080/13816810.2020.1868011. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Epicanthal Folds, Strabismus, Hypotonia, and Brown Syndrome. Dr. Couser is board certified in American Board Of Medical Genetics And Genomics and American Board Of Ophthalmology.

Ambroise Wonkam is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Wonkam is rated as an Experienced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Anemia, Fragile X Syndrome, Pyle Disease, and Micrognathia.

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 Branchio-Oculo-Facial Syndrome (BOFS). 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. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019. She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias. Dr. Hoover is rated as an Experienced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 26 other conditions, according to our data. Her clinical expertise encompasses Rhizomelic Syndrome, Achondroplasia, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy. Dr. Hoover is board certified in American Board Of Medical Genetics And 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 Branchio-Oculo-Facial Syndrome (BOFS). 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.

Benjamin Darbro is a Medical Genetics provider practicing medicine in Iowa City, Iowa. Dr. Darbro is rated as an Experienced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Malignant Peripheral Nerve Sheath Tumor, Osteomyelitis in Children, Neu Laxova Syndrome, and Non-Muscle Invasive Bladder Cancer.

Helio Pedro is a Pediatrics provider practicing medicine in Hackensack, New Jersey. Dr. Pedro is rated as an Experienced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Glycine Encephalopathy, Biotinidase Deficiency, Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia. Dr. Pedro is board certified in American Board Of Medical Genetics And Genomics.

Touran Zadeh is a Pediatrics provider practicing medicine in Orange, California. She has been practicing medicine for over 53 years. Dr. Zadeh is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 31 other conditions, according to our data. Her clinical expertise encompasses Branchio-Oculo-Facial Syndrome (BOFS), Ring Chromosome 7, Ring Chromosome 18, and Ring Chromosome 14. Dr. Zadeh is board certified in American Board Medical Genetics.

Olaf Bodamer is a Medical Genetics provider practicing medicine in Boston, Massachusetts. Dr. Bodamer is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Microcephaly. Dr. Bodamer is currently accepting new patients.

Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Sacharow is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 158 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.

Amelle Shillington is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Cincinnati, Ohio. Dr. Shillington is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 161 other conditions, according to our data. Her clinical expertise encompasses Chromosome 13q Deletion, Hardikar Syndrome, Yunis-Varon Syndrome, and Frank Ter Haar Syndrome. Dr. Shillington is currently accepting new patients.

Mayra Ojeda is a Pediatrics provider practicing medicine in Winter Park, Florida. Dr. Ojeda is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Branchio-Oculo-Facial Syndrome (BOFS), Focal or Multifocal Malformations in Neuronal Migration, and Neurofibromatosis Type 1 (NF1).

Robert Hopkin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Cincinnati, Ohio. Dr. Hopkin is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 207 other conditions, according to our data. His clinical expertise encompasses Fabry Disease, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Microcephaly, and Orchiectomy.

David Harris is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Harris is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Cat Eye Syndrome, Branchio-Oculo-Facial Syndrome (BOFS), Congenital Athymia, and Autism Spectrum Disorder. Dr. Harris is currently accepting new patients.

Howard Saal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Cincinnati, Ohio. Dr. Saal is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). He is also highly rated in 200 other conditions, according to our data. His clinical expertise encompasses Achondroplasia, Treacher Collins Syndrome, Acrofacial Dysostosis Rodriguez Type, and Acrofacial Dysostosis Catania Type.

Anne Slavotinek is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Cincinnati, Ohio. Dr. Slavotinek is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 146 other conditions, according to our data. Her clinical expertise encompasses Chromosome 13q Deletion, Tetrasomy 9p, Mosaic Variegated Aneuploidy Syndrome, and Temple Syndrome. Dr. Slavotinek is currently accepting new patients.

Sun Kim is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Orleans, Louisiana. Dr. Kim is rated as an Advanced provider by MediFind in the treatment of Branchio-Oculo-Facial Syndrome (BOFS). She is also highly rated in 37 other conditions, according to our data. Her clinical expertise encompasses Chromosome 13q Deletion, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, and Cat Eye Syndrome.