Crawford JS (1970) Congenital fibrosis syndrome. Can J Ophthalmol 5:331–336
PubMed
Google Scholar
Heuk G (1879) Ueber angeborenen vererbten Beweglichkeitsdefekt der Augen. Klin Monatsbl Augenheilkd 17:253–278
Google Scholar
Harley RD, Rodrigues MM, Crawford JS (1978) Congenital fibrosis of the extraocular muscles. Trans Am Ophthalmol Soc 26:198–226
Google Scholar
Engle EC, Kunkel LM, Specht LA, Beggs AH (1994) Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12. Nat Genet 7:69–73
PubMed
Google Scholar
Engle EC, Marondel I, Houtman WA, de Vries B, Loewenstein A, Lazar M, Ward DC, Kucherlapati R, Beggs AH (1995) Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): Genetic homogeneity, linkage refinement, and physical mapping on chromosome 12. Am J Hum Genet 57:1086–1094
CAS
PubMed
Google Scholar
Engle EC, Goumernov B, McKeown CA, et al (1997) Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles. Ann Neurol 41:314–325
CAS
PubMed
Google Scholar
Wang SM, Zwaan J, Mullaney PB, Jabak MH, Al-Awad A, Beggs AH, Engle EC (1998) Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13. Am J Hum Genet 63:517–525
Article
PubMed
Google Scholar
Nakano M, Yamada K, Fain J, Sener EC et al (2001) Homozygous mutations in ARIX (PHOXA) result in congenital fibrosis of the extraocular muscles type 2. Nat Genet 29:315–320
Article
CAS
PubMed
Google Scholar
Pattyn A, Morin X, Cremer H, Goridis C, Brunet JF (1997) Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis. Development 124:4065–4075
CAS
PubMed
Google Scholar
Guo S, Brush J, Teraoka H, Goddard A, Wilson SW, Mullins MC, Rosenthal A (1999) Development of noradrenergic neurons in the zebrafish hindbrain requires BMP, FGF8, and the homeodomain protein soulless/Phox2a. Neuron 24:555–566
CAS
PubMed
Google Scholar
Doherty EJ, Macy ME, Wang SM, Dykeman CP, Melanson MT, et al (1999) CFEOM3: A new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3. Invest Ophthalmol Vis Sci 40:687–694
Google Scholar
Abeloos MC, Cordonnier M, Van Nechel C, Van Bogaert P, Gerard JM, Van Regemoorter N (1990) Congenital fibrosis of the ocular muscles: a diagnosis for several clinical pictures. Bull Soc Belge Ophtalmol 24:61–74
Google Scholar
Brodsky MC (1998) Hereditary external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation. Ophthalmology 105:717–725
PubMed
Google Scholar
Appleton RE, Chitayat D, Jan JE, Kennedy R, Hall JG (1989) Joubert's Syndrome associated with congenital ocular fibrosis and histidinemia. Arch Neurol 46:579–582
PubMed
Google Scholar
Jacobson DM, Johnson R, Frens DB (1992) Joubert's syndrome, ocular fibrosis, and normal histidine levels. Am J Ophthalmol 113:714–716
PubMed
Google Scholar
Flaherty M, Grattan-Smith P, Steinberg A, Jamieson R, Engle E (2001) Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia. Ophthalmology 108:1313–1322
Article
PubMed
Google Scholar
Gottlob I, Jain S, Engle EC (2002) Elevation of one eye during tooth brushing. Am J Ophthalmol 134:459–460
Article
PubMed
Google Scholar
Brigell M, Bach M, Barber C, Kawasaki K, Kooijman A (1998) Guidelines for calibration of stimulus and recording parameters used in clinical electrophysiology of vision. Calibration Standard Committee of the International Society for Clinical Electrophysiology of Vision (ISCEV). Doc Ophthalmol 95:1–14
Google Scholar
Brodsky MC, Pollock SC, Buckley DG (1989) Neural misdirection in congenital ocular fibrosis Syndrome: implications and pathogenesis. J Pediatr Ophthalmol Strabismus 26:159–161
PubMed
Google Scholar
Pratt SG, Beyer CK, Johnson CC (1984) The Marcus Gunn phenomenon: A review of 71 cases. Ophthalmology 90:27–30
Google Scholar
Beyer-Machule CK, Johnson CC, Pratt SG, et al (1985) The Marcus-Gunn phenomenon. Orbit 4:15
Google Scholar
Mrabet A, Oueslati S, Gazzah H, Ben Hamida M (1991) Clinical and electrophysiological study of 2 familial cases of Marcus Gunn phenomenon. Rev Neurol 147:215–219
PubMed
Google Scholar
Kirkham TH (1969) Familial Marcus Gunn phenomenon. Br J Ophthalmol 53:282–283
PubMed
Google Scholar
Leyten QH, Gabreels FJ, Renier WO, ter Laak HJ (1996) Congenital muscle dystrophy: a review of the literature. Clin Neurol Neurosurg 98:267–280
Article
PubMed
Google Scholar
Saraiva JM, Baraitser M (1992) Joubert syndrome: a review. Am J Med Genet 43:726–731
PubMed
Google Scholar
Joubert M, Eisenring JJ, Robb JP, Andermann F (1969) Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation. Neurology 19:813–825
PubMed
Google Scholar
Lambert SR, Kriss A, Gresty M, Benton S, Taylor D (1989) Joubert syndrome. Arch Ophthalmol 107:624–631
CAS
Google Scholar
Dekaban AS (1969) Hereditary syndrome of congenital retinal blindness (Leber), polycystic kidneys and maldevelopment of the brain. Am J Ophthalmol 68:1029–1036
PubMed
Google Scholar
Jeret JS, Serur D, Wisniewski KE, Lubin RA (1987) Clinicopathological findings associated with agenesis of the corpus callosum. Brain Dev 9:255–264
PubMed
Google Scholar
Calogero JA (1977) Vermian agenesis and unsegmented midbrain tectum. Case report. J Neurosurg 47:605–608
PubMed
Google Scholar
Suzuki H, Nakazoto A, Ikota H, et al (1983) A case of Joubert syndrome: CT findings of brain stem and review of literature. Brain Dev 15:67–73
CAS
Google Scholar