The Rieger syndrome: Orofacial manifestations. Case report of a rare condition

Quintessence International

Volumn 34, Issue 9, 2003, Pages 689-692

  Singh, Jagjit ^a   Pannu, Karneev ^a   Lehl, Gurvanit ^a  

^a GOVERNMENT MEDICAL COLLEGE AND HOSPITAL   (India)

Author keywords

Autosomal dominant disorder; Craniofacial anomaly; Genetic disorder; Oligodontia; Rieger anomaly

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DENTURE; EYE MALFORMATION; GLAUCOMA; HUMAN; IRIS; MALE; MAXILLA; MOUTH EXAMINATION; PATHOLOGY; PHYSICAL EXAMINATION; RETROGNATHIA; RIEGER SYNDROME; SYNDROME; TOOTH EXTRACTION; TOOTH MALFORMATION; VISUAL IMPAIRMENT;

ADULT; DENTURE, PARTIAL, FIXED; EYE ABNORMALITIES; GLAUCOMA; HUMANS; IRIS; MALE; MAXILLA; RETROGNATHISM; SYNDROME; TOOTH ABNORMALITIES;

EID: 0141729311     PISSN: 00336572     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

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