The Library of Congress > LCCN Permalink

View this record in:  MARCXML | LC Authorities & Vocabularies

Axenfeld-Rieger syndrome

LC control no.sh2005002992
Topical headingAxenfeld-Rieger syndrome
    Browse this term in  LC Authorities  or the  LC Catalog
Variant(s)Axenfeld anomaly
Rieger anomaly
See alsoEye--Abnormalities
    Browse this term in  LC Authorities
Genetic disorders
    Browse this term in  LC Authorities
Skull--Abnormalities
    Browse this term in  LC Authorities
Syndromes
    Browse this term in  LC Authorities
Found inWork cat.: 2005012665: The molecular mechanisms of Axenfeld-Rieger syndrome, c2005: CIP galley (Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant disorder. The cardinal features of ARS include specific ocular anomalies of the anterior segment, dental anomalies and periumbilical skin)
Multiple congenital anomaly/mental retardation (MCA/MR) syndromes database via WWW, May 13, 2005 (Axenfeld-Rieger syndrome: Axenfeld anomaly (defect of peripheral segment of the eye) and Rieger anomaly (defect of the anterior segment of the eye) associated with variable craniofacial abnormalities, abnormal dentition, ... and mental retardation)
Handbook of Ocular Disease Management via WWW, May 13, 2005 (Axenfeld-Rieger Syndrome)