Congenital fibrosis syndrome associated with central nervous system abnormalities

Graefe's Archive for Clinical and Experimental Ophthalmology

Volumn 241, Issue 7, 2003, Pages 546-553

  Pieh, Christina ^a   Goebel, Hans Hilmar ^b   Engle, Elizabeth C ^c   Gottlob, Irene ^d  

^a CANTONAL HOSPITAL ST GALLEN   (Switzerland)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d UNIVERSITY OF WARWICK   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN DEVELOPMENT; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; CEREBELLUM VERMIS; CHILD; CHROMOSOME ANALYSIS; CONGENITAL STRABISMUS; CORPUS CALLOSUM AGENESIS; DISEASE ASSOCIATION; ELECTRORETINOGRAPHY; ENCEPHALOCELE; EXTRAOCULAR MUSCLE; EYE MOVEMENT; GENE MUTATION; GENETIC LINKAGE; HISTOLOGY; HUMAN; INFANT; LINKAGE ANALYSIS; MALE; MYOFIBROSIS; NEUROLOGIC EXAMINATION; NEURORADIOLOGY; OCULAR FIBROSIS; OCULOMOTOR NERVE; OCULOMOTOR NERVE DISEASE; OPHTHALMOPLEGIA; PACHYGYRIA; PRIORITY JOURNAL; TROCHLEAR NERVE DISEASE;

BLEPHAROPTOSIS; CENTRAL NERVOUS SYSTEM; CHILD; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; EYE MOVEMENTS; FIBROSIS; HUMANS; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; NERVOUS SYSTEM MALFORMATIONS; OCULOMOTOR MUSCLES; OPHTHALMOPLEGIA; SYNDROME;

EID: 0042563041     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-003-0703-z     Document Type: Article

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