Rieger-Axenfeld anomaly (Q58533): Difference between revisions
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Síndrome Axenfeld-Rieger (ARS) é um termo genérico usado para designar transtornos genéticos sobrepostos, em que a maior condição física é a disgenesia do segmento anterior do olho. Pacientes com ARS também podem apresentar múltiplas e variáveis anomalias congênitas (dismorfismo craniofacial leve, anomalias dentárias e pele periumbilical redundante). | |||
| description / en | description / en | ||
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). | |||
Revision as of 06:06, 14 August 2026
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). |
