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Journal Article
Journal of Glaucoma, ISSN 1057-0829, 03/2018, Volume 27, Issue 6, pp. e110 - e112
BACKGROUND:Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor receptor 2 and 3 (FGFR2 and FGFR3) genes... 
congenital glaucoma | anterior segment dysgenesis | glaucoma | Crouzon syndrome | ANTERIOR-CHAMBER DYSGENESIS | MUTATION | OPHTHALMOLOGY | CRANIOSYNOSTOSIS | Glaucoma | Complications and side effects | Risk factors | Craniofacial dysostosis
Journal Article
Journal Article
Bulletin de l'Academie Nationale de Medecine, ISSN 0001-4079, 04/2017, Volume 201, Issue 4-6, pp. 631 - 637
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 08/1997, Volume 81, Issue 8, pp. 639 - 643
AIMS/BACKGROUND Females with Turner syndrome commonly exhibit ophthalmological abnormalities, although there is little information in the literature... 
K SU OPHTHALMOLOGY | OPHTHALMOLOGY | CHIMERISM | ITO | ASSOCIATION | HYPOMELANOSIS | Descemet Membrane - abnormalities | Humans | Karyotyping | Anterior Chamber - abnormalities | Turner Syndrome - genetics | Female | Infant | Mosaicism - genetics | Glaucoma - genetics | Index Medicus | Original articles - Clinical science
Journal Article
BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE, ISSN 0001-4079, 04/2017, Volume 201, Issue 4-6, pp. 631 - 635
Chronic glaucoma is well known in adults due to the insidious alteration in the visual field as well as acute glaucoma due to its brutality, unbearable pain... 
APOTOSIS | NEURAL CRESTS | MEDICINE, GENERAL & INTERNAL | CONGENITAL GLAUCOMA | EYE'S ANTERIOR CHAMBER DYSGENESIS
Journal Article
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 06/1995, Volume 206, Issue 6, pp. 474 - 476
Background Sclerocornea is a congenital, uni- or bilateral, non-progressive, non-inflammatory malformation characterized by histological changes of the cornea... 
CORNEAL ECTASIA | OPHTHALMOLOGY | SCLEROCORNEA | ELECTRON MICROSCOPY | ANTERIOR CHAMBER DYSGENESIS | HISTOPATHOLOGY
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 06/1995, Volume 206, Issue 6, p. 474
Journal Article
Ceskoslovenska oftalmologie, ISSN 0009-059X, 02/1990, Volume 46, Issue 1, p. 69
The authors present an account on a 12-year-old girl with ectomesodermal dysgenesis of the Rieger type syndrome. The disease was manifested at the age of nine... 
Abnormalities, Multiple - pathology | Humans | Karyotyping | Anterior Chamber - abnormalities | Female | Child | Abnormalities, Multiple - genetics | Syndrome
Journal Article
American Journal of Medical Genetics, ISSN 0148-7299, 07/1999, Volume 85, Issue 2, pp. 160 - 170
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 05/1990, Volume 196, Issue 5, pp. 279 - 284
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 1973, Volume 76, Issue 4, pp. 462 - 467
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 1995, Volume 206, Issue 6, pp. 474 - 476
Journal Article
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