Literature DB >> 15097252

Gonioscopic findings in patients with type 1 neurofibromatosis (Von Recklinghausen disease).

Luciano Quaranta1, Francesco Semeraro, Raffaele Turano, Enrico Gandolfo.   

Abstract

PURPOSE: Based on the known neurocristopathic etiology of type 1 neurofibromatosis (NF1) and the neuroectodermal embryologic derivation of the iridocorneal angle, we examined a sample of young patients affected with NF1 to see if they have evidence of underdevelopment of the angular region. PATIENTS AND METHODS: We designed a case-controlled clinical study. Forty-two consecutive patients (42 eyes), 24 male and 18 female, affected with NF1 were recruited for the study. Forty-two eyes of 42 consecutive young patients (19 male and 23 female) served as a control group for the iridocorneal angle features studied. Indirect gonioscopy was performed by the means of a Goldmann lens. The intraocular pressure was measured with a Goldmann applanation tonometer. Photographs were taken of the anterior segment and of all the four quadrants of the iridocorneal angle to record the presence of abnormalities. The iridocorneal angle was graded according to the classification proposed by Spaeth. Evaluation of the angle also included the gonioscopic width of ciliary body band (CBB).
RESULTS: In this study we found that 29 of 42 eyes (69%) of the NF1 group had mild anteriorization, even if within normal limits, of the iris insertion and abundant basal iris processes. The CBB was either invisible (54.84%) or very narrow (21.4%). Three NF1 patients had bilateral juvenile congenital glaucoma.
CONCLUSIONS: It seems that patients affected with NF1 often have characteristic gonioscopic findings consistent with underdevelopment of the iridocorneal angle.

Entities:  

Mesh:

Year:  2004        PMID: 15097252     DOI: 10.1097/00061198-200404000-00002

Source DB:  PubMed          Journal:  J Glaucoma        ISSN: 1057-0829            Impact factor:   2.503


  5 in total

1.  Ciliary body cysts in neurofibromatosis: a new coexistence?

Authors:  Sinan Emre; Melis Palamar; M Oğuz Ulusoy; Gülsüm Gençoğlan
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2011-10-06       Impact factor: 3.117

Review 2.  [Congenital glaucoma and neurofibromatosis type 1].

Authors:  Nazih Tzili; Hamza El Orch; Fatiha Bencherifa; Mohammed Charif Chefchaouni; El Hassan Abdallah; Amina Berraho
Journal:  Pan Afr Med J       Date:  2015-05-25

3.  A rare case of primary congenital glaucoma in combination with neurofibromatosis 1: a case report.

Authors:  Haijun Li; Ting Liu; Xia Chen; Lin Xie
Journal:  BMC Ophthalmol       Date:  2015-10-29       Impact factor: 2.209

4.  Clinical features and outcome of corneal opacity associated with congenital glaucoma.

Authors:  Yu Jeong Kim; Jin Wook Jeoung; Mee Kum Kim; Ki Ho Park; Young Suk Yu; Joo Youn Oh
Journal:  BMC Ophthalmol       Date:  2018-08-02       Impact factor: 2.209

5.  Progressive ectropion uveae and secondary angle-closure glaucoma in type 1 neurofibromatosis.

Authors:  Hamed Esfandiari; Janice Lasky Zeid; Angelo P Tanna
Journal:  Am J Ophthalmol Case Rep       Date:  2022-02-02
  5 in total

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