MarkCEddyMD

Pediatric Endocrinology • Saint Louis, MO

Associate Professor, Pediatrics, St Louis University School of Medicine

Join to view full profile

Dr. Eddy is on Doximity

As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.

Connect with other colleagues in the same hospital or clinic
Search all U.S. specialist profiles and refer a patient
Read the latest clinical news and earn CME/CEU credits

See Dr. Eddy's full profile

Already have an account?

Office
1465 S Grand
Saint Louis, MO 63104
Phone+1 314-577-5648

Fax+1 314-268-6448
Is this information wrong?

Education & Training

Washington University/B-JH/SLCH ConsortiumFellowship, Pediatric Endocrinology, 1994 - 1997
Children’s Mercy HospitalResidency, Pediatrics, 1991 - 1994
University of Missouri-Columbia School of MedicineClass of 1991

Certifications & Licensure

IL State Medical License 1998 - 2026
MO State Medical License 1998 - 2025
American Board of Pediatrics Pediatrics

Awards, Honors, & Recognition

Fellow (FAAP) American Academy of Pediatrics

Publications & Presentations

PubMed

2 citations
Polycystic Bone Disease
Michael P. Whyte, Mark C. Eddy, Michelle N. Podgornik, William H. McAlister> ;Journal of Bone and Mineral Research. 2010 Feb 18
2 citations
Newborn metabolic screening and related pitfalls.
Mark C. Eddy, Gary S. Gottesman> ;Missouri Medicine. 2009 May 1
5 citations
Pseudo-(Tumor-Induced) Rickets
Michael P. Whyte, Michelle N. Podgornik, Valerie A. Wollberg, Mark C. Eddy, William H. McAlister> ;Journal of Bone and Mineral Research. 2001 Aug 1
54 citations
Expansile skeletal hyperphosphatasia: a new familial metabolic bone disease.
Michael P. Whyte, Barbara G. Mills, William R. Reinus, Michelle N. Podgornik, G. David Roodman, Francis H. Gannon, Mark C. Eddy, William H. McAlister> ;Journal of Bone and Mineral Research. 2000 Dec 1
74 citations
Deficiency of the α‐Subunit of the Stimulatory G Protein and Severe Extraskeletal Ossification
Mark C. Eddy, Suzanne M. Jan de Beur, Suzanne M. Yandow, William H. McAlister, Eileen M. Shore, Frederick S. Kaplan, Michael P. Whyte, Michael A. Levine> ;Journal of Bone and Mineral Research. 2000 Nov 1
6 citations
Polycystic bone disease: A new, autosomal dominant disorder.
Michael P. Whyte, Mark C. Eddy, Michelle N. Podgornik, William H. McAlister> ;Journal of Bone and Mineral Research. 1999 Aug 1
32 citations
x-linked Recessive Spondyloepiphyseal Dysplasia Tarda Clinical and Radiographic Evolution in a 6-generation Kindred and Review of the Literature
Michael P. Whyte, Gary S. Gottesman, Mark C. Eddy, William H. McAlister> ;Medicine. 1999 Jan 1
6 citations
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasia.
Mark C. Eddy, Robert D. Steiner, William H. McAlister, Michael P. Whyte> ;American Journal of Medical Genetics. 1998 May 18
12 citations
X-linked hypophosphatemia: Normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-induced renal azotemia☆
Mark C. Eddy, William H. McAlister, Michael P. Whyte> ;Bone. 1997 Dec 1
7 citations
Erratum: metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndrome (Pediatr radiol (1997) 27: 436-441)
Thomas E. Herman, A. Chines, William H. McAlister, Gary S. Gottesman, Mark C. Eddy, Michael P. Whyte> ;Pediatric Radiology. 1997 Nov 1
45 citations
Calcinosis universalis complicating juvenile dermatomyositis: resolution during probenecid therapy
Mark C. Eddy, Rattana Leelawattana, William H. McAlister, Michael P. Whyte> ;The Journal of Clinical Endocrinology and Metabolism. 1997 Nov 1
11 citations
Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndrome
Thomas E. Herman, A. Chines, William H. McAlister, Gary S. Gottesman, Mark C. Eddy, Michael P. Whyte> ;Pediatric Radiology. 1997 May 1
Join now to see all