The 20 Best Rhizomelic Syndrome Doctors Near Me

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 Elite provider by MediFind in the treatment of Rhizomelic Syndrome. 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.

Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober is rated as an Elite provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 70 other conditions, according to our data. His clinical expertise encompasses Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is board certified in American Board Of Medical Genetics And Genomics.

Wedad Fallatah is a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Fallatah is rated as an Elite provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, Achondrogenesis, and Acromesomelic Dysplasia.

Nancy Braverman is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Braverman is rated as an Elite provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.

Erminia Di Pietro practices practicing medicine in Montreal, Canada. Ms. Di Pietro is rated as an Elite expert by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Zellweger Syndrome, X-Linked Chondrodysplasia Punctata 2, Chondrodysplasia Punctata Syndrome, and Achondrogenesis.

Andjela Drincic is an Endocrinologist practicing medicine in Omaha, Nebraska. She has been practicing medicine for over 36 years. Dr. Drincic is rated as an Experienced provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 30 other conditions, according to our data. Her clinical expertise encompasses Type 1 Diabetes (T1D), Pituitary Tumor, Hypogonadism, and Type 2 Diabetes (T2D).

Michael Mannstadt is an Endocrinologist practicing medicine in Boston, Massachusetts. Dr. Mannstadt is rated as a Distinguished provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Hypoparathyroidism, Mccune-Albright Syndrome, Autosomal Dominant Hypocalcemia, Hormone Replacement Therapy (HRT), and Thyroidectomy.

Naim Maalouf is an Endocrinologist practicing medicine in Dallas, Texas. Dr. Maalouf is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 29 other conditions, according to our data. His clinical expertise encompasses Milk-Alkali Syndrome, Hypercalcemia, Hyperparathyroidism, Parathyroidectomy, and Ureteroscopy.

Dr. Nara Lygia De Macena Sobreira is an assistant professor at the McKusick-Nathans Department of Genetic Medicine at Johns Hopkins University School of Medicine. Her area of expertise is rare Mendelian phenotypes, analysis of next-generation sequencing, and functional testing of candidate causative variants. She earned her M.D. at the University of Pernambuco in Brazil. She finished her Ph.D. in Human Genetics at Johns Hopkins followed by a one-year postdoc also at Johns Hopkins School of Medicine. During her Ph.D., she worked with Dr. David Valle using next-generation sequencing to elucidate the molecular basis of rare Mendelian phenotypes and in 2010 she discovered PTPN11 as the gene responsible for metachondromatosis by using whole-genome sequencing. She completed residencies in clinical genetics at both Universidade Federal de Sao Paulo and Johns Hopkins. Her main clinical and research focus is on identifying the genetic bases of rare phenotypes, mainly, phenotypes associated with cartilage tumors and vascular anomalies (including Ollier disease and Maffucci syndrome), and on understanding the physiopathology of these phenotypes to identify pharmacological strategies to treat them. She has worked extensively on developing strategies to better analyze the variants identified by next-generation sequencing and on novel strategies for data sharing. She participated on the development of PhenoDB, a phenotypic and genomic database, and created PhenoDB Variant Analysis Tool used worldwide. She is also one of the creators of GeneMatcher, VariantMatcher, and one of the co-founders of the Matchmaker Exchange, all intended to share next-generation sequencing data. She has also worked extensively on functional studies that evaluate the possible pathogenic effects of the candidate causative variants. Recent News Articles and Media Coverage Living the Hopkins Mission Honorees, Johns Hopkins Medicine Successes in Characterizing Genes through GeneMatcher with Nara L. M. Sobreira, MD, PhD, Ambry Genetics (April 30, 2018) Enfermedades raras: el desafio es encontrar otros pacientes que tienen el mismo mal, Lun (26 de septiembre de 2019) 2021 Science Writers' Boot Camp, Johns Hopkins Medicine (June 7, 2021) Making the Perfect Match, Johns Hopkins Medicine (February 1, 2020). Dr. De Macena Sobreira is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 24 other conditions, according to our data. Her clinical expertise encompasses Spondyloepimetaphyseal Dysplasia Strudwick Type, Greenberg Dysplasia, Blepharophimosis, and Early Infantile Epileptic Encephalopathy. Dr. De Macena Sobreira is board certified in American Board Of Medical Genetics And Genomics.

Dr. Edward Hsiao is an endocrinologist who specializes in metabolic bone diseases, such as severe osteoporosis and osteogenesis imperfecta, and other bone disorders. He also cares for patients with calcium, phosphorous, vitamin D, and parathyroid hormone disorders. He has particular interests in fibrodysplasia ossificans progressiva (a condition in which bone gradually replaces muscle and other connective tissues) and fibrous dysplasia/McCune-Albright syndrome (a disorder that causes fibrous tissue to develop in bones). E. Hsiao's current research interests center on understanding how hormones and signaling pathways control human bone formation. His laboratory uses advanced cellular, genetic, and bioengineering tools to identify key pathways that could be targeted for disease therapies. He is also involved in clinical research to develop better diagnostic and treatment strategies for patients with bone diseases. E. Hsiao earned his medical degree and a doctorate in molecular biology and genetics from the Johns Hopkins School of Medicine, where he also completed a residency in internal medicine. He completed fellowship training in diabetes, endocrinology and metabolism at UCSF. E. Hsiao is a member of the Endocrine Society and American Society for Bone and Mineral Research. In addition, he actively works with patient support groups through the Fibrous Dysplasia Foundation and International Fibrodysplasia Ossificans Progressiva Association, and the International Clinical Council on FOP. E. Hsiao serves as director of UCSF's fellowship program in diabetes, endocrinology and metabolism. He has received the March of Dimes Basil O'Connor Starter Scholar Research Award and the Doris Duke Clinical Scientist Development Award, as well as research grant funding from the National Institutes of Health. In his free time, Hsiao enjoys reading, the outdoors and photography. Dr. Hsiao is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Fibrous Dysplasia, Osteitis Fibrosa, Mccune-Albright Syndrome, and Rhizomelic Syndrome. Dr. Hsiao is board certified in American Board Of Internal Medicine, Endocrinology Diabetes & Metab. Dr. Hsiao is currently accepting new patients.

Richard Haas is an Endocrinologist practicing medicine in Worcester, Massachusetts. He has been practicing medicine for over 49 years. Dr. Haas is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Type 1 Diabetes (T1D), and Mccune-Albright Syndrome. Dr. Haas is board certified in Endocrinology-Diabetes and Internal Medicine.

Juan Pallais is an Endocrinologist practicing medicine in Boston, Massachusetts. Dr. Pallais is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Hyperparathyroidism, Addison's Disease, Secondary Adrenal Insufficiency, and Osteoporosis. Dr. Pallais is board certified in Endocrinology, Diabetes And Metabolism.

Pryia Dayamani is an Endocrinologist practicing medicine in Atlanta, Georgia. Dr. Dayamani is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 23 other conditions, according to our data. Her clinical expertise encompasses Anaplastic Thyroid Cancer, Medullary Thyroid Carcinoma, Follicular Thyroid Cancer, and Papillary Thyroid Cancer.

Henry Bone is an Endocrinologist practicing medicine in Detroit, Michigan. He has been practicing medicine for over 54 years. Dr. Bone is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Osteoporosis, Postmenopausal Osteoporosis, Paget's Disease of Bone, and Hyperparathyroidism. Dr. Bone is board certified in American Board Of Internal Medicine and American Board Of Internal Medicine. Dr. Bone is currently accepting new patients.

Mona Al Mukaddam is an Endocrinologist practicing medicine in Philadelphia, Pennsylvania. Dr. Al Mukaddam is rated as an Advanced provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Osteoporosis, Postmenopausal Osteoporosis, Juvenile Primary Osteoporosis, Hypothyroidism, and Fasciotomy.

Lisa Kratz is a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Kratz is rated as a Distinguished provider by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Greenberg Dysplasia, Smith-Lemli-Opitz Syndrome, Rhizomelic Syndrome, and Chondrodysplasia Punctata Syndrome.

Katta Girisha practices practicing medicine in Manipala, India. Girisha is rated as a Distinguished expert by MediFind in the treatment of Rhizomelic Syndrome. They are also highly rated in 79 other conditions, according to our data. Their clinical expertise encompasses Pyle Disease, Brachydactyly Mononen Type, Arthrogryposis Multiplex Congenita, and Congenital Contractures.

Philippe Campeau practices practicing medicine in Montreal, Canada. Mr. Campeau is rated as a Distinguished expert by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 67 other conditions, according to our data. His clinical expertise encompasses DOOR Syndrome, Argininosuccinic Aciduria, Micrognathia, and Craniofacial-Deafness-Hand Syndrome.

Joanna Sztulpa-Walczak practices practicing medicine in Poznan, Poland. Ms. Sztulpa-Walczak is rated as a Distinguished expert by MediFind in the treatment of Rhizomelic Syndrome. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Cranioectodermal Dysplasia, Epicanthal Folds, Clouston Syndrome, Aplasia Cutis Congenita, and Kidney Transplant.

Fabian Dorninger practices practicing medicine in Vienna, Austria. Mr. Dorninger is rated as a Distinguished expert by MediFind in the treatment of Rhizomelic Syndrome. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Rhizomelic Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Refsum Disease.