Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension;Morphologie, familienanamnese und diagnosezeitpunkt bei 26 patienten mit Axenfeld-Rieger-syndrom und glaukom oder okulärer hypertension

Ophthalmologe

Volumn 103, Issue 5, 2006, Pages 393-400

  Dressler P ^a   Gramer, E ^a  

^a UNIVERSITY HOSPITAL WÜRZBURG   (Germany)

Author keywords

Axenfeld Rieger syndrome; Dental anomalies; Genetics; Glaucoma; Iris hypoplasia

Indexed keywords

AGE; ARTICLE; AXENFELD RIEGER SYNDROME; CHILD; CLINICAL ARTICLE; EARLY DIAGNOSIS; EYE MALFORMATION; FACE MALFORMATION; FAMILY HISTORY; GENETICS; GLAUCOMA; GLAUCOMA SURGERY; HUMAN; INTRAOCULAR HYPERTENSION; INTRAOCULAR PRESSURE; IRIS DISEASE; IRIS HYPOPLASIA; MORPHOLOGY; PROGNOSIS; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 13; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; FORKHEAD TRANSCRIPTION FACTORS; GENES, DOMINANT; GENETIC SCREENING; GLAUCOMA; HOMEODOMAIN PROTEINS; HUMANS; IRIS; MANOMETRY; MAXILLOFACIAL ABNORMALITIES; OCULAR HYPERTENSION; PROGNOSIS; RETROSPECTIVE STUDIES; SYNDROME; TOOTH ABNORMALITIES; TRANSCRIPTION FACTORS;

EID: 33646555717     PISSN: 0941293X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00347-006-1335-6     Document Type: Article

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