Dr. Patricia Gordon

Dr. Bellus is a board-certified and fellowship-trained specialist in clinical genetics. His clinical interests include skeletal dysplasia and genetic skin disorders. Dr. Bellus attended the University of Colorado, where he received his medical degree. He completed his residency at St. Louis Children's Hospital, a fellowship at Johns Hopkins University School of Medicine and another fellowship at the University of Colorado Health Sciences Center. Dr. Bellus is certified by the American Board of Medical Genetics and Genomics and by the American Board of Pediatrics.|In his personal life, Dr. Bellus enjoys woodworking and playing guitar. He earned his bachelor's degree in biology from Columbia College in New York City, and his PhD in molecular biology from the University of Connecticut Health Sciences Center in Farmington, Conn. Dr. Bellus likes to volunteer at patient support group camps. Dr. Bellus is rated as an Experienced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). His top areas of expertise are Cortical Dysplasia, Uncombable Hair Syndrome, Neurofibromatosis, and Neurofibromatosis Type 1 (NF1).

Ashutosh Kumar is a Pediatrics specialist and a Neurologist in Hershey, Pennsylvania. Dr. Kumar is rated as an Advanced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). His top areas of expertise are Diabetic Neuropathy, Severe Acute Respiratory Syndrome (SARS), Seizures, Nerve Decompression, and Laminectomy.

Dr. Seeley is a board-certified and fellowship-trained specialist in pediatric genetics. She earned her medical degree from Thomas Jefferson University. She completed her residency as well as a fellowship in pediatrics and medical genetics at the University of Michigan Hospitals and Health Centers. Dr. Seeley is certified by the American Board of Medical Genetics and Genomics and by the American Board of Pediatrics. Dr. Seeley is rated as an Advanced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Glutaric Acidemia Type 2, Fountain Syndrome, Beta-Ketothiolase Deficiency, and Acrodysostosis.