Familial Arnold-Chiari Type I malformation [14]

Eye

Volumn 20, Issue 3, 2006, Pages 400-402

  George, Sonja ^a   Page, A B ^a  

^a ROYAL VICTORIA HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BRONCHODILATING AGENT; PHENYTOIN;

ABDUCENS NERVE PARALYSIS; ADULT; AMBLYOPIA; ARNOLD CHIARI MALFORMATION; ASTHMA; BINOCULAR CONVERGENCE; BRAIN HERNIA; CASE REPORT; CLINICAL FEATURE; CONVERGENT STRABISMUS; DECOMPRESSION SURGERY; DEMYELINATING DISEASE; DIFFERENTIAL DIAGNOSIS; DIPLOPIA; DISEASE ASSOCIATION; FASCICULATION; FEMALE; FOCAL EPILEPSY; HEADACHE; HUMAN; HYPERREFLEXIA; INTRAOCULAR PRESSURE; LABORATORY DIAGNOSIS; LETTER; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; OPHTHALMOSCOPY; SIBLING; SYRINGOMYELIA; VISUAL ACUITY; VISUAL FIELD;

EID: 33646266725     PISSN: 0950222X     EISSN: 14765454     Source Type: Journal    
DOI: 10.1038/sj.eye.6701887     Document Type: Letter

References (5)

1. Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert CM et al. Chiari I malformation redefined: Clinical, radiographic and genetic features in 364 symptomatic patients. Neurosurgery 1999; 44: 1005-1017.
2. Speer MC, George TM, Enterline DS, Franklin A, Wolpert CM, Milhorat TH. A genetic hypothesis for Chiari I malformation with or without syringomyelia. Neurosurg Focus 2000; 8(3) Article 12: 1-4.
3. Herman MD, Cheek WR, Storrs BB. Two siblings with the Chiari I malformation. Pediatr Neurosurg 1990-91; 16: 183-184.
4. Gimenez-Roldan S, Benito C, Mateo D. Familial communicating syringomyelia. J Neurolog Sci 1978; 36: 135-146.
5. Gripp KW, Scott Jr CI, Nicholson L, Magram G, Grissom L. Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda. Skeletal Radiol 1997; 26: 131-133.