Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome (ARS) is a generic term used to designate overlapping genetic disorders, in which the major physical condition is anterior segment dysgenesis of the eye. Patients with ARS may also present with multiple variable congenital anomalies.

Micrognathia

Developmental hypoplasia of the mandible.


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PMID (PMCID)
3117999
 MALE Infant
The Rieger syndrome and a chromosome 13 deletion.
Stathacopoulos RA, Bateman JB, Sparkes RS, Hepler RS.
J Pediatr Ophthalmol Strabismus. 1987;24(4):198-203.
We studied a boy with the ocular features of the Rieger syndrome, micrognathia, and redundancy of the periumbilical skin.