My philosophy is to provide compassionate and personalized care. I like to engage children and their parents in developing the best treatment plan for them.
Nat Nasomyont, MD, MS

About

Biography

As a pediatric endocrinologist, I provide comprehensive care for children and adolescents with hormone disorders, including growth and puberty problems, thyroid diseases and diabetes. I also evaluate and treat metabolic bone diseases and osteoporosis in childhood and adolescents.

My philosophy is to provide compassionate and personalized care. I like to engage children and their parents in developing the best treatment plan for them. I am board certified by the American Board of Pediatrics (2017) and Pediatric Endocrinology (2021). As a Certified Clinical Densitometrist (2020), I also provide service in bone density analysis as part of a comprehensive bone health evaluation.

My current research focuses on bone health in children and adolescents with conditions that may predispose them to a compromised peak bone mass. Childhood and adolescence are critical periods for bone mass accrual. I hope my work on the early identification and intervention for children at risk for low bone mass will ultimately prevent osteoporosis during their adult years.

MD: Siriraj Hospital Faculty of Medicine, Bangkok, Thailand, 2011.

Residency: Pediatrics, University of South Alabama, Mobile, AL, 2017.

Fellowship: Pediatric Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2020.

MS: Clinical and Translational Research, University of Cincinnati, Cincinnati, OH, 2020.

Certification: American Board of Pediatrics, 2017; Pediatric Endocrinology, 2021; Certified Clinical Densitometrist (CCD), 2020.

Interests

Pediatric endocrinology; metabolic bone disease; pediatric osteoporosis; diabetes

Services and Specialties

Endocrinology

Interests

Metabolic bone disease; pediatric osteoporosis

Research Areas

Endocrinology

Insurance Information

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Publications

Selected

Outcomes following intravenous bisphosphonate infusion in pediatric patients: A 7-year retrospective chart review. Nasomyont, N; Hornung, LN; Gordon, CM; Wasserman, H. Bone. 2019; 121:60-67.

Elevated bone turnover markers predict bone mineral density accrual in adolescents with 21-hydroxylase deficiency. Wiromrat, P; Namphaisan, P; Wongsurawat, N; Panamonta, O; Nasomyont, N. Clinical Endocrinology. 2023; 99:462-469.

Bone Mineral Density and Dickkopf-1 in Adolescents with Non-Deletional Hemoglobin H Disease. Wiromrat, P; Rattanathongkom, A; Laoaroon, N; Suwannaying, K; Komwilaisak, P; Panamonta, O; Wongsurawat, N; Nasomyont, N. Journal of Clinical Densitometry. 2023; 26:101379.

Successful Treatment of Hypoglycemia With Alpelisib in Pediatric Patients With PIK3CA-Related Overgrowth Spectrum. Nasomyont, N; Rutter, MM; Backeljauw, PF. 2023; 1:luad027.

Changes in Bone Marrow Adipose Tissue in Transgender and Gender Non-Conforming Youth Undergoing Pubertal Suppression: A Pilot Study. Nasomyont, N; Meisman, AR; Ecklund, K; Vajapeyam, S; Cecil, KM; Tkach, JA; Altaye, M; Corathers, SD; Conard, LA; Kalkwarf, HJ; et al. Journal of Clinical Densitometry. 2022; 25:485-489.

The effect of oral bisphosphonate therapy on vertebral morphometry and fractures in patients with Duchenne muscular dystrophy and glucocorticoid-induced osteoporosis. Nasomyont, N; Tian, C; Hornung, L; Khoury, J; Hochwalt, PM; Tilden, JC; Wong, BL; Rutter, MM. Muscle and Nerve. 2021; 64:710-716.

Chapter 37 Osteoporosis in childhood and adolescence. Nasomyont, N; Gordon, CM. Marcus and Feldman's Osteoporosis. : Elsevier; Elsevier; 2021.

Safety and efficacy of teriparatide treatment for severe osteoporosis in patients with Duchenne muscular dystrophy. Nasomyont, N; Keefe, C; Tian, C; Hornung, L; Khoury, J; Tilden, JC; Hochwalt, P; Jackson, E; Rybalsky, I; Wong, BL; et al. Osteoporosis International. 2020; 31:2449-2459.

Intravenous bisphosphonate therapy in children with spinal muscular atrophy. Nasomyont, N; Hornung, LN; Wasserman, H. Osteoporosis International. 2020; 31:995-1000.

Central Diabetes Insipidus in a Patient With NFKB2 Mutation: Expanding the Endocrine Phenotype in DAVID Syndrome. Nasomyont, N; Lindsley, AW; Assa'ad, A; Dawson, DB; Neilson, DE; Brady, CC; Rutter, MM. Journal of Clinical Endocrinology and Metabolism. 2019; 104:4051-4057.

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4.6
Overall Patient Rating