Acrodysostosis

Definition

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.

Alternative Names

Arkless-Graham; Acrodysplasia; Maroteaux-Malamut

Causes

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.

Symptoms

Exams and Tests

Your health care provider can usually diagnose this condition with a physical exam.

This may show:

In the first months of life, x-rays may show spotty calcium deposits, called stippling, in bones (especially the nose). Infants may also have:

Treatment

Treatment depends on the symptoms.

Orthopedic care, early intervention, and special education are recommended.

Outlook (Prognosis)

Problems depend on the degree of skeletal involvement and intellectual disability. In general, patients do relatively well.

Possible Complications

When to Contact a Medical Professional

Call your health care provider if your infant or child does not seem to be growing or developing properly.

Prevention

Genetic counseling may be helpful.


Review Date: 11/2/2012
Reviewed By: 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.
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