International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia

Achondroplasia is the most common skeletal dysplasia and is characterized by a variety of medical, functional and psychosocial challenges across the lifespan. There is variability in…

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What is the Role for Pediatric Endocrinologists in the Management of Skeletal Dysplasias?

Despite the recognized expertise of pediatric endocrinologists, children with skeletal dysplasias have not been consistently managed by these physicians. Growth-altering treatments have broadened the role of…

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Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study- a multicenter retrospective cohort study of achondroplasia in the US

Achondroplasia growth charts included in this article. Achondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/dwarfism. Common additionalfeatures include spinal stenosis, midface retrusion,…

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Constitutional Growth Delay

Constitutional Growth Delay and Familial Short Stature: A Guide for Families What is Short Stature? Doctors usually define short stature based on standard growth charts, rather…

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Child with Suspected Short Stature

Primary Care provider guidelines for referral.

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Cost-Conscious Growth-Promoting Treatment: When Discretion Is the Better Part of Value (HRP 2018)

A mini-review on cost-conscious growth-promoting treatment.

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GH Deficiency, Idiopathic Short Stature, and IGF-I Deficiency Treatment Guidelines (HRP 2016)

PES Drugs and Therapeutics and Ethics committees present guidelines for Growth Hormone and Insulin-like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I Deficiency.

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Use of Aromatase Inhibitors in Children and Adolescents with Disorders of Growth and Adolescent Development (Pediatrics 2008)

A review of published data regarding the use of aromatase inhibitors in pediatrics.

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Changes in Recombinant Human Growth Hormone Prescribing Information (PES D & T Committee 2008)

Members of the Drug and Therapeutics Committee of the Lawson Wilkins Pediatric Endocrine Society describe the changes in the prescribing information for the different forms of
rhGH.

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Growth Hormone (GH) Treatment to Final Height in Children with Idiopathic Short Stature: Evidence for a Dose Effect (The Journal of Pediatrics)

An open-label randomized study analyzing the effect of two doses of growth hormone (GH) on final height and height velocity during the first 2 years of treatment of children with idiopathic short stature.

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