Anterior segment dysgenesis with glaucoma and systemic anomalies.
- Specialty
- Ophthalmology
- Subspecialty
- Ophthalmology / Glaucoma
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, congenital
- Gene(s) involved
- FOXC1, FOXO1, PITX2, PRDM5
- Alternative names & eponyms
- Axenfeld–Rieger anomaly
Etiology & mechanism
Neural crest developmental defect.
Gene(s) involved (4)
Symptoms & signs (7)
In plain terms, someone with Axenfeld–Rieger syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Alagille syndrome
posterior embryotoxon
1 shared
Fuchs heterochromic iridocyclitis syndrome
glaucoma
1 shared
Lowe syndrome
glaucoma
1 shared
Nail-patella syndrome
glaucoma
1 shared
Nail–patella syndrome
glaucoma
1 shared
Peters plus syndrome
glaucoma
1 shared
Pseudoexfoliation syndrome
glaucoma
1 shared
Sturge–Weber syndrome
glaucoma
1 shared
Weill–Marchesani syndrome
glaucoma
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