Acrodysostosis is an extremely rare disorder that is present at birth (congenital). It leads to problems with the bones of the hands, feet, and nose, and intellectual disability.
Arkless-Graham; Acrodysplasia; Maroteaux-Malamut
Causes, incidence, and risk factors
Most patients with acrodysostosis have no family history of the disease. However, sometimes the condition is passed down from parent to child. Parents with the condition have a 1 in 2 chance of passing the disorder to their children.
There is a slightly greater risk with fathers who are older.
Worsening range of movement in the spine, elbows, and hands
Calling your health care provider
Call your health care provider if your infant or child does not seem to be growing or developing properly.
Genetic counseling may be helpful.
Chad Haldeman-Englert, MD, FACMG, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, David R. Eltz, and Stephanie Slon.
are leaving the St. Francis Health Center/Sisters of Charity of Leavenworth
Health System website. Persons visiting this external site assume full
responsibility for use of its information and agree that St. Francis/SCLHS is
not responsible or liable for claim, loss/damage arising from this use or for
the content of any external site. Your use of any external site is subject to
our full disclaimer.