Rieger-Axenfeld anomaly (Q58533)
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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 (mild craniofacial dysmorphism, dental anomalies and redundant periumbilical skin).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1338180594 |
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| English | Rieger-Axenfeld anomaly |
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 (mild craniofacial dysmorphism, dental anomalies and redundant periumbilical skin). |
Statements
CID11:ID_1338180594
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dki-india-ID_1338180594
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