Alport syndrome: A review

Clinical Eye and Vision Care

Volumn 12, Issue 3-4, 2000, Pages 139-150

  McCarthy, Patricia A ^a   Maino, Dominick M ^a  

^a ILLINOIS COLLEGE OF OPTOMETRY   (United States)

Author keywords

Alport syndrome; Cataracts; Deafness; Developmental delay; Early intervention programs; Flecked retinopathy; Hereditary nephritis; Lenticonus

Indexed keywords

ALPORT SYNDROME; COPING BEHAVIOR; HUMAN; OPTOMETRY; PERCEPTION DEAFNESS; QUALITY OF LIFE; REFRACTION ERROR; RETINOPATHY; REVIEW; SYSTEMIC DISEASE; TREATMENT PLANNING;

EID: 0034538474     PISSN: 09534431     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0953-4431(00)00042-4     Document Type: Review

References (56)

1. Alport syndrome
2. Alport's syndrome
3. Inherited diseases of the glomerular basement membrane
4. Idiopathic or congenital, hereditary and family hematuria
5. Hereditary familial congenital haemorrhagic nephritis
6. Renal disease, inner ear deafness, and ocular changes
7. Alport's syndrome: Review and case report
8. Retinal abnormalities in Alport's syndrome
9. Macular lesions in Alport's disease
10. Alport's syndrome - Ocular manifestations and unusual features
11. Ocular manifestations of Alport's syndrome: A hereditary disorder of basement membranes?
12. Alport's syndrome and the eye
13. Ocular finding in Alport's syndrome
14. An electrophysiological study on children and young adults with Alport's syndrome
15. Clinical features and pathogenesis of Alport retinopathy
16. Type IV collagen a5 chain: Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody
17. Identification of a distinct type IV collagen a chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome
18. Molecular cloning of a5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus
19. Type IV collagen: Structure, gene organization, and role in human diseases
20. Structure of the human type IV collagen COL4A5 gene
21. Molecular genetics of Alport syndrome: The clinical consequences
22. Molecular genetics of Alport's syndrome
23. Lens coloboma and Alport-like glomerulonephritis
24. Alport's syndrome or hereditary nephritis?
25. The role of optometry in early intervention
26. Social integration: Assessment and intervention with regard to students who are deaf
27. Psychological long-term coping with experience of disease and treatment in childhood cancer survivors
28. Lens capsule abnormalities in Alport's syndrome
29. Alport syndrome: From bedside to genome to bedside
30. Alport's syndrome: Specificity and pathogenesis of glomerular basement membrane alterations
31. Pathologic characteristics of hereditary nephritis
32. Immunohistologic studies of type IV collagen in anterior lens capsules of patients with Alport syndrome
33. Identification of mutations in the COL4A5 collagen gene in Alport syndrome
34. Alport's syndrome: Can carriers be identified by audiometry?
35. Erroneous genetic risk assessment of Alport syndrome
36. Familial oesophgeal leiomyomatosis and nephropathy
37. Alport-leiomyomatosis syndrome: An update
38. Ocular signs in Alport's syndrome
39. Recurrent corneal epithelial erosions in Alport's syndrome
40. Behavioural disturbance as a manifestation of ocular disease in children
41. Anterior lenticonus in familial hemorrhagic nephritis
42. Pigment dispersion in a case of Alport's syndrome
43. Alport's syndrome and retinal telangiectasia
44. Ocular manifestations of various systemic disorders
45. Hereditary macular dystrophies
46. Hereditary pigmentary degenerations of the retina
47. Toxic retinopathies
48. Fundus changes in the hereditary nephropathies
49. High-risk children referred to an early-intervention developmental program
50. Psychologic reactions of children to physical illness
51. Effect of cyclosporin A on proteinuria in patients with Alport's syndrome
52. Renal transplantation from living donor parents in two brothers with Alport syndrome
53. Glaucoma associated with corneal disorders
54. Clear lens extraction and intraocular lens implantation in a patient with bilateral anterior lenticonus secondary to Alport's syndrome
55. Clear lens extraction for anterior lenticonus