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Article

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.

Ophthalmology - 1 Nov 1996

Walter M A, Mirzayans F, Mears A J, Hickey K, Pearce W G

Abstract excerpt

PURPOSE: To determine whether there is a locus for iridogoniodysgenesis (IGD)/ familial iris hypoplasia in the region of the known Axenfeld-Rieger syndrome (ARS) locus at 4q25 and to determine the ocular phenotype within the autosomal-dominant iris hypoplasia group of disorders. METHODS: Clinical examinations were performed on 27 members, with 11 affected from one family in which the IGD occurred in association...

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PMID: 8942889
DOI: 10.1016/s0161-6420(96)30408-9

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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