Rare Bone Disease TeleECHO Clinic Series
The Osteogenesis Imperfecta Foundation and the Rare Bone Disease Alliance are excited to announce the Rare Bone Disease TeleECHO Clinic Series. The goal of this educational program, a partnership with Project ECHO™ (Extension for Community Healthcare Outcomes), is to build capacity to safely and effectively diagnose and treat rare bone diseases and disorders.
The full schedule with links to register for specific session topics is listed below. Participants can also sign up to receive program reminders and updates here.
This series uses Zoom video conferencing and will take place on the first Thursday of every month at 3pm EST. In each monthly session, faculty members or guest speakers present a brief didactic presentation, followed by participant-led case presentations and group discussion of the presented cases. The faculty encourages participants to present case studies related to rare bone diseases at each session. Recordings of each didactic presentation are posted after each session.
The Rare Bone TeleECHO Clinic Series is intended for medical professionals and clinicians who treat patients with rare bone diseases to improve their differential diagnosis skills and provide up-to-date evaluation and management strategies. Click here to view the program flyer.
The interdisciplinary faculty in the Rare Bone Disease TeleECHO includes:
Michael Collins, MD National Institutes of Health, NIDCR
Michael Lewiecki, MD University of New Mexico
Eric Rush, MD University of Kansas Hospital
Jay Shapiro, MD Uniformed Services University of Health Sciences
Dolores Shoback, MD University of California San Francisco
Laura Tosi, MD Children’s National Health System
In support of improving patient care, Project ECHO® is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Project ECHO® designates this live activity for a maximum of 1.0 AMA PRA Category 1 CreditsTM. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
The program schedule below includes recordings of past didactic presentations and links to register for individual sessions of the Rare Bone Disease ECHO program.
August 6, 2020; 3:00pm EST
RECORDING: Melorheostosis: The Genes Behind the Dripping Candle Wax
Timothy Bhattachyrra, MD Orthopaedic Surgery, NIAMS/NIH
September 3, 2020; 3:00pm EST
RECORDING: Evaluation of Patients with Hyperphosphatemia
Michael Collins, MD Senior Investigator, Skeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research/NIH
October 1, 2020; 3:00pm EST
RECORDING: Mechanisms of Bone Loss in Complex Lymphatic Anomalies
Michael Kelly, MD, PhD Professor of Pediatrics, Northeast Ohio Medical University
November 5, 2020; 3:00pm EST
RECORDING: Dental Concerns in Patients with Rare Bone Disorders
Tim Wright, DDS, MS Bawden Distinguished Professor, Division of Pediatrics and Public Health, Adams School of Dentistry, University of North Carolina
December 3, 2020; 3:00pm EST
RECORDING: Generalized Arterial Calcification of Infancy (GACI)
Carlos Ferreira, MD Chief, Skeletal Genomics Unit, National Human Genome Research Institute, NIH
January 7, 2021; 3:00pm EST
RECORDING: Skeletal Surveys – A Systematic Approach
Dorothy Bulas, MD Chief, Department of Radiology, Children’s National Hospital; Professor of Pediatrics and Radiology, George Washington University School of Medicine
February 4, 2021; 3:00pm EST
RECORDING: Jansen’s Disease
Harald Jueppner, MD Chief, Pediatric Nephrology, Massachusetts General Hospital; Professor of Pediatrics, Harvard Medical School
March 4, 2021; 3:00pm EST Register for this session.
Bone Pain in Children
Alison Boyce, MD Associate Research Physician, National Institute of Dental and Craniofacial Research, NIH
April 1, 2021; 3:00pm EST Register for this session.
Multiple Hereditary Exostoses
David S. Feldman, MD Co-Director, Multiple Hereditary Exostoses Center, St. Mary’s Medical Center, West Palm Beach, FL
May 6, 2021; 3:00pm EST Register for this session
DXA Evaluation in the Child
Catherine Gordon, MD Adolescent Chief, Boston Children’s Hospital; Robert P. Masland, Jr. Chair of Adolescent Medicine, Professor of Pediatrics, Harvard Medical School
June 3, 2021; 3:00pm EST Register for this session.
Kathryn Dahir, MD Professor of Medicine, Vanderbilt University Medical Center
July 1, 2021; 3:00pm EST Register for this session.
Evaluation of the Child with Multiple Fractures
Eric. T. Rush, MD, FAAP, FACMG Clinical Geneticist, Children’s Mercy Kansas City; Associate Professor of Pediatrics, University of Missouri-Kansas City School of Medicine; Clinical Associate Professor of Medicine, University of Kansas School of Medicine
Genetic Testing in the Diagnosis of Rare Bone Disease – Eric Rush MD, FAAP, FACMG
Associate Professor of Medicine at the University of Kansas Medical Center and Associate Professor of Pediatrics at University of Missouri – Kansas City
OI Dominant vs Recessive: Impact on Treatment – Reid Sutton MD
Medical Director of Biochemical Genetics Laboratory, Director of Medical Genetics Residency Program and ABMGG Diagnostic Laboratory Training Program at Baylor College of Medicine, and Director of Inborn Errors of Metabolism Service at Texas Children’s Hospital
Hypocalcemia – Dolores Shoback MD
Professor of Medicine and Director of the UCSF Training Program in Diabetes, Endocrinology, and Metabolism at the University of California San Francisco (UCSF) Health
Fibrous Dysplasia – McCune Albright – Michael Collins MD
Senior Clinical Investigator, Skeletal Disorders, and Mineral Homeostasis Section at NIH NIDCR
Non-Accidental Trauma – Peter Byers MD
Professor of Medicine, Pathology, and Medical Genetics at University of Washington Medicine
XLH Disorders – Thomas Carpenter MD
Professor of Pediatric Endocrinology, Orthopaedics, and Rehabilitation, Clinical Professor of Nursing, Director of the Yale Center for X-Linked Hypophosphatemia (XLH), and Medical Director of the Hospital Research Unit at Yale School of Medicine
Diagnostic Approach to the Child with a Skeletal Dysplasia – Julie Hoover-Fong MD, PhD
Director of the Greenberg Center for Skeletal Dysplasias and Professor of Pediatrics at Johns Hopkins Medicine
Hypophosphatasia – Michael Whyte MD
Medical Director at the Center for Metabolic Bone Disease and Molecular Research at Shriners Hospitals for Children — St. Louis and Professor of Medicine, Pediatrics, and Genetics at Washington University School of Medicine
Evaluation of the Child with Rickets – Erik Imel MD
Associate Professor of Medicine and Pediatrics at Indiana University School of Medicine
Osteopetrosis – Michael Econs MD
Professor of Medical & Molecular Genetics and Division Chief of Endocrinology and Metabolism at Indiana University School of Medicine
Fibrodysplasia Ossificans Progressiva – Edward Hsiao MD, PhD
Associate Professor of Medicine at University of California San Francisco (UCSF) Health
July 2, 2020
Management of Pregnancy & Delivery in the Patient with a Skeletal Disorder – Deborah Krakow, MD Chair of the Department of Obstetrics and Gynecology, Professor of Orthopaedic Surgery, and Professor of Human Genetics at University of California Los Angeles (UCLA) Health