Health Supervision for People With Achondroplasia

Author:

Hoover-Fong Julie1,Scott Charles I.2,Jones Marilyn C.3,Chen Emily,Trotter Tracy L.,Berry Susan A.,Burke Leah W.,Geleske Timothy A.,Hamid Rizwan,Hopkin Robert J.,Introne Wendy J.,Lyons Michael J.,Scheuerle Angela,Stoler Joan M.,

Affiliation:

1. Greenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;

2. Nemours/Alfred I. duPont Hospital for Children and Sidney Kimmel Medical College, Thomas Jefferson University, Wilmington, Delaware; and

3. Department of Pediatrics, University of California, San Diego and Rady Children’s Hospital, San Diego, California

Abstract

Achondroplasia is the most common short-stature skeletal dysplasia, additionally marked by rhizomelia, macrocephaly, midface hypoplasia, and normal cognition. Potential medical complications associated with achondroplasia include lower extremity long bone bowing, middle-ear dysfunction, obstructive sleep apnea, and, more rarely, cervicomedullary compression, hydrocephalus, thoracolumbar kyphosis, and central sleep apnea. This is the second revision to the original 1995 health supervision guidance from the American Academy of Pediatrics for caring for patients with achondroplasia. Although many of the previously published recommendations remain appropriate for contemporary medical care, this document highlights interval advancements in the clinical methods available to monitor for complications associated with achondroplasia. This document is intended to provide guidance for health care providers to help identify individual patients at high risk of developing serious sequelae and to enable intervention before complications develop.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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