Congenital symblepharon (abortive cryptophthalmos) associated with meningoencephalocele
- Author
- GÜNDÜZ, K1 ; GÜNALP, I2
[1] Mevki Military Hospital, Ankara, Turkey
[2] Ocular Oncology Department, Eye Clinic, Faculty of Medicine, University of Ankara, Ankara, Turkey - Source
Ophthalmic plastic and reconstructive surgery. 1997, Vol 13, Num 2, pp 139-141 ; ref : 14 ref
- CODEN
- OPRSEU
- ISSN
- 0740-9303
- Scientific domain
- Ophthalmology
- Publisher
- Lippincott Williams and Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Adolescent Association Congénital Cryptophtalmie Encéphalocèle Etude cas Symblépharon Encéphale pathologie Homme Maladie congénitale Malformation Oeil pathologie Paupière pathologie Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Adolescent Association Congenital Cryptophtalmia Encephalocele Case study Symblepharon Cerebral disorder Human Congenital disease Malformation Eye disease Eyelid disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Adolescente Asociación Congénito Criptoftalmia Encefalocele Estudio caso Blefarosinequia Encéfalo patología Hombre Enfermedad congénita Malformación Ojo patología Párpado patología Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B09 Ophthalmology / 002B09A Malformations of the eye
- Discipline
- Ophthalmology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2681096
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1097/00002341-199706000-00009 
https://dx.doi.org/10.1097/00002341-199706000-00009
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