Evaluation of short stature

Last reviewed: 8 Apr 2025
Last updated: 17 Jul 2024

Summary

Differentials

Common

  • Familial short stature (genetic short stature)
  • Constitutional delay of growth and development
  • Idiopathic short stature
  • Small for gestational age (SGA) without catch-up growth by 2 years of age
Full details

Uncommon

  • Growth hormone (GH) deficiency
  • Hypothyroidism
  • Cushing syndrome
  • GH insensitivity (Laron syndrome)
  • Craniopharyngioma
  • Turner syndrome
  • Noonan syndrome
  • Russell-Silver syndrome
  • Trisomy 21
  • Prader-Willi syndrome (PWS)
  • DiGeorge syndrome (velocardiofacial syndrome)
  • Celiac disease
  • Cystic fibrosis (CF)
  • Asthma (moderate or severe)
  • Chronic heart disease (congenital or acquired)
  • Diabetes mellitus
  • Chronic kidney failure
  • Juvenile idiopathic arthritis (JIA)
  • Crohn disease
  • Ulcerative colitis
  • Malignancy
  • Renal tubular acidosis
  • Rickets
  • Skeletal dysplasias (e.g., achondroplasia, hypochondroplasia, osteogenesis imperfecta)
  • Spinal disorders (irradiation, surgery, congenital deformities)
  • Psychosocial deprivation (abuse, neglect, starvation, institutionalization)
  • Anorexia nervosa
  • Bulimia nervosa
  • Fetal alcohol syndrome
  • Stimulant medications for ADHD
Full details

Contributors

Authors

Renee Bargman, MS, MD
Renee Bargman

Pediatric Endocrinology

NYC Health and Hospitals/SUNY Downstate Medical Center

Brooklyn

NY

Disclosures

RB declares that she has no competing interests.

Acknowledgements

Dr Renee Bargman would like to gratefully acknowledge Dr Maria Vogiatzi, a previous contributor to this topic.

Peer reviewers

Ian Marshall, MD

Chief of the Division of Pediatric Endocrinology

Assistant Professor

UMDNJ-Robert Wood Johnson Medical School

New Brunswick

NY

Disclosures

IM declares that he has no competing interests.

Raphael David, MD

Professor of Pediatrics

Director

Pediatric Endocrinology

New York University Medical Center

New York

NY

Disclosures

RD declares that he has no competing interests.

References

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Key articles

Wit JM, Kamp GA, Oostdijk W, et al. Towards a rational and efficient diagnostic approach in children referred for growth failure to the general paediatrician. Horm Res Paediatr. 2019;91(4):223-40.Full text  Abstract

Cooke R, Goulet O, Huysentruyt K, et al. Catch-up growth in infants and young children with faltering growth: expert opinion to guide general clinicians. J Pediatr Gastroenterol Nutr. 2023 Jul 1;77(1):7-15.Full text  Abstract

Cohen P, Rogol AD, Deal CL, et al. Consensus statement on the diagnosis and treatment of children with idiopathic short stature: a summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop. J Clin Endocrinol Metab. 2008 Nov;93(11):4210-7.Full text  Abstract

Bryant J, Baxter L, Cave CB, et al. Recombinant growth hormone for idiopathic short stature in children and adolescents. Cochrane Database Syst Rev. 2007 Jul 18;(3):CD004440.Full text  Abstract

Reference articles

A full list of sources referenced in this topic is available to users with access to all of BMJ Best Practice.

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