Literature DB >> 6789269

Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata.

R A Lewis, V M Riccardi.   

Abstract

The results of a prospective survey of the ophthalmic manifestations of neurofibromatosis (NFT) have never been published. We studied the ocular features of NFT in 77 patients (ages 5 weeks to 69 years) among whom the diagnosis was made by nonophthalmic parameters. Of subjects ages 6 years and older, 92% had hamartomatous lesions of the iris, termed Lisch nodules, as distinguished from common iris nevi in nonaffected individuals. The presence of Lisch nodules is correlated to age, but not to number of café-au-lait spots, number of neurofibromata, or severity of disease. Lisch nodules appear among prepubertal children and are apparently unique to NFT. They are a valuable criterion by which to diagnose NFT in problematic cases.

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Mesh:

Year:  1981        PMID: 6789269     DOI: 10.1016/s0161-6420(81)35034-9

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  23 in total

1.  A novel pattern of oculocerebral malformation.

Authors:  B J Clark; W R Lee; D Doyle; R Arngrimsson; J L Tolmie; J B Stephenson
Journal:  Br J Ophthalmol       Date:  1997-06       Impact factor: 4.638

2.  Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous features.

Authors:  F Faravelli; M Upadhyaya; M Osborn; S M Huson; R Hayward; R Winter
Journal:  J Med Genet       Date:  1999-12       Impact factor: 6.318

3.  Ophthalmic manifestations of neurofibromatosis.

Authors:  S Huson; D Jones; L Beck
Journal:  Br J Ophthalmol       Date:  1987-03       Impact factor: 4.638

4.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.

Authors:  S M Huson; D A Compston; P Clark; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

Review 5.  Recent developments in the diagnosis and management of neurofibromatosis.

Authors:  S M Huson
Journal:  Arch Dis Child       Date:  1989-05       Impact factor: 3.791

6.  Uveal malignant melanoma and optic nerve glioma in von Recklinghausen's neurofibromatosis.

Authors:  C M Antle; K F Damji; V A White; J Rootman
Journal:  Br J Ophthalmol       Date:  1990-08       Impact factor: 4.638

Review 7.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Authors:  S M Huson; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

8.  A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1.

Authors:  Sean Boley; Jennifer L Sloan; Alexander Pemov; Douglas R Stewart
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-06-10       Impact factor: 4.799

9.  Combined hamartoma of the retina and retinal pigment epithelium associated with neurofibromatosis type-1.

Authors:  R N Vianna; D F Pacheco; M M Vasconcelos; J J de Laey
Journal:  Int Ophthalmol       Date:  2001       Impact factor: 2.031

10.  Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): a follow-up study.

Authors:  A Fois; L Calistri; P Balestri; R Vivarelli; G Bartalini; L Mancini; A Berardi; M Vanni
Journal:  Eur J Pediatr       Date:  1993-06       Impact factor: 3.183

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