Ocular changes in mucopolysaccharidosis IV A (Morquio A syndrome) and long-term results of perforating keratoplasty

Ophthalmologica

Volumn 213, Issue 3, 1999, Pages 200-205

  Käsmann Kellner, Barbara ^a   Weindler, Josef ^a   Pfau, Britta ^a   Ruprecht, Klaus W ^a  

^a SAARLAND UNIVERSITY   (Germany)

Author keywords

Child; Keratoplasty; Low vision; Morquio A syndrome; Mucopolysaccharidosis

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CORNEA OPACITY; ELECTROPHYSIOLOGY; HUMAN; MALE; MORQUIO SYNDROME; NIGHT BLINDNESS; NYSTAGMUS; OPTIC NERVE ATROPHY; PENETRATING KERATOPLASTY; TAPETORETINAL DEGENERATION; TREATMENT OUTCOME; VISUAL ACUITY;

EID: 0344061544     PISSN: 00303755     EISSN: None     Source Type: Journal    
DOI: 10.1159/000027420     Document Type: Article

References (13)

1. Beck M, Glossl J, Grubisic A, Spranger J: Heterogeneity of Morquio disease. Clin Genet 1991;29:325-332.
2. Maroteaux P, Stanescu V: Hétérogéneité des formes de la maladie de Morquio. Arch Fr Pédiatr 1982;39:761-765.
3. Maumenee I: The cornea in connective tissue diseases. Ophthalmology 1978;85:1014-1019.
4. Morquio L: Sur une forme de dystrophie osseuse familiale. Bull Soc Pédiatr Paris 1929;27: 145-152.
5. O'Brien JS, Gugler E, Giedion A, Weismann R, Herschkowitz N, Meier C, Leroy JC: Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiency. Clin Genet 1976;9:495-504.
6. Von Noorden GK, Zellweger H, Ponseti I: Ocular findings in Morquio-Ulrich disease. Arch Ophthalmol 1960;64:585-591.
7. Baker E, Guo XH, Osborn AM, Sutherland GR, Gallen DF, Hopwood JJ, Morris CP: The Morquio A syndrome (mucopolysaccharidosis IV A) gene maps to 16q24.3. Am J Hum Genet 1993;52:96-98.
8. Cahane M, Treister G, Abraham FA, Melamed S: Glaucoma in sibling with Morquio syndrome. Br J Ophthalmol 1990;74:382-383.
9. Iwamoto M, Nawa Y, Maumenee IH, Young-Ramsaran J, Matalon R, Green WR: Ocular histopathology and ultrastructure of Morquio syndrome (systemic mucopolysaccharidosis IV A). Graefes Arch Clin Exp Ophthalmol 1990; 228:342-349.
10. Olsen H, Baggesen K, Sjolie AK: Cataracts in Morquio syndrome (mucopolysaccharidosis IV A). Ophthalmic Pediatr Genet 1993;14:87-89.
11. Piccirilli CB, Chadduck WM: Cervical kyphotic myelopathy in a child with Morquio syndrome. Childs Nerv Syst 1996;12:114-116.
12. Takano T, Yamanouchi Y: Assignment of human beta-galactosidase-A gene to 3p21.33 by fluorescence in situ hybridization. Hum Genet 1993;92:403-404.
13. Naumann GOH, Rummelt V: Aufklaren der transplantatnahen Wirtshornhaut nach perforierender Keratoplastik beim Maroteaux-Lamy-Syndrom (Mukopolysaccharidose Typ VIA). Klin Monatsbl Augenheilkd 1993;203: 351-360.