[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address Please contact the publisher to request reinstatement.
[Skip to Content Landing]
October 1983

Picture of the Month

Author Affiliations

Contributed from the Department of Pediatrics, Rhode Island Hospital, Providence.

Am J Dis Child. 1983;137(10):1017-1018. doi:10.1001/archpedi.1983.02140360077021

Denouement and Discussion 

Frontometaphyseal Dysplasia 

Manifestations  Frontometaphyseal dysplasia is an uncommon syndrome that consists of skeletal and dental anomalies, a distinctive facial appearance, and hearing loss.Affected patients appear normal at birth, but gradually abnormal facial features develop during early childhood. The most characteristic abnormality is enlargement and thickening of the supraorbital areas. The chin may be small and/or pointed. Dental anomalies can be extensive, involving delayed eruption, missing permanent teeth, and retained deciduous teeth. Height and weight are generally normal, although the patients have an unusual habitus with a mildly shortened trunk and long thin upper limbs and fingers. There may be flexion deformities of the elbows, hands, and feet that tend to progress. Hearing loss is of a mixed conductive and sensorineural type and is also progressive. Other skeletal problems include chest cage deformities, winging of the scapulae, abnormalities of the cervical