General Fibrosis Syndrome (Congenital Enophthalmos
with Ocular Muscle Fibrosis and Ptosis;
Congenital Fibrosis of the Inferior Rectus with Ptosis; Strabismus Fixus;
Vertical Re 252i86c traction
Syndrome (Congenital Fibrosis Syndrome )
General: Present from birth; familial history; apparent autosomal dominant transmission; sex-linked recessive transmission also reported.
Ocular: Ptosis; enophthalmos; disk hypoplasia; astigmatism; esotropia; exotropia; hypotropia; nystagmus; visual loss; positive forced duction test; may be associated with Marcus Gunn jaw-winking and synergistic divergence in attempted right gaze.
Clinical: None.
Brodsky MC, et al. Neural misdirection in congenital ocular fibrosis syndrome: implications and pathogenesis. J Pediatr Ophthalmol Strabismus 1989; 26:159.
Fraunfelder FT, Roy FH. Current Ocular Therapy. 5th ed. Philadelphia: WB Saunders, 2000.
Harley RD, et al. Congenital fibrosis of the extraocular muscles. J Pediatr Ophthalmol Strabismus 1978; 15:346-358.
Kim, JH, Hwang JM: Hypoplastic oculomotor nerve in congenital fibrosis syndrome and synergistic divergence with magnetic resonance imaging. Ophthalmology 2005; 112: 728-
Miller NR, ed. Walsh and Hoyt's Clinical Neuro-Ophthalmology. vol. 2. 4th ed. Baltimore: Williams & Wilkins, 1985.
Yazdani A, Traboulsi EI: Classification and surgical management of patients with familial and sporadic forms of congenital fibrosis of the extraocular muscles. Ophthalmology 2004; 111: 1035-l042.
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