Literature DB >> 7886862

The blinding mechanisms of incontinentia pigmenti.

M F Goldberg1.   

Abstract

Five case histories illustrate the disabling visual diseases caused by retinal and cerebral infarction in incontinentia pigmenti. Cortical blindness was definitely present in one baby, who had bilateral absence of light perception, and was probably present in a second infant also. Retinal detachment occurred in three eyes of three patients, one of whom had spontaneous reattachment. In a second patient, a partial tractional retinal detachment progressed within 4 months during infancy to a total, inoperable, retrolental, white fibrovascular mass mimicking stage 5 retinopathy of prematurity. Phthisis bulbi resulted. In a third patient, a localized tractional retinal detachment originated at the nonperfused macula and extended over a 7-month period to the ora serrata. Preretinal neovascularization waxed and waned in these and other patients. Abnormalities of the macula were pronounced but were sometimes difficult to detect. Their severity and relative frequency have not been previously described in detail. Abnormalities included blunting or absence of the foveal pit and absence of the normal foveal avascular zone. One patient at 12 days of age had an infarcted macula with a cherry-red spot. Similar episodes may have occurred in other children and would be sufficient to explain the appearance of macular abnormalities and otherwise unexplainable poor visual acuity in older individuals. Well-focused macular angiography appears to be highly useful in explaining visual disability due to abnormal foveal anatomy and function. Optic atrophy occurred in several eyes. Its pathogenesis may be multifactorial. Further research is necessary to elucidate the mechanisms of vascular closure in the retina as well as the pathogenesis of destructive encephalopathy in this exceptionally severe disease. Valid therapeutic possibilities may then become more obvious than they are at present. It is possible that the retina and brain undergo similar disease processes in incontinentia pigmenti.

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Year:  1994        PMID: 7886862      PMCID: PMC1298505     

Source DB:  PubMed          Journal:  Trans Am Ophthalmol Soc        ISSN: 0065-9533


  10 in total

1.  Treatment of proliferative retinopathy associated with incontinentia pigmenti.

Authors:  R A Catalano; M Lopatynsky; W S Tasman
Journal:  Am J Ophthalmol       Date:  1990-12-15       Impact factor: 5.258

2.  [Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case].

Authors:  C Triki; D Devictor; S Kah; M Roge-Wolter; C Lacroix; P Y Venencie; P Landrieu
Journal:  Rev Neurol (Paris)       Date:  1992       Impact factor: 2.607

3.  Retinal detachments in incontinentia pigmenti.

Authors:  K J Wald; M C Mehta; O Katsumi; N R Sabates; T Hirose
Journal:  Arch Ophthalmol       Date:  1993-05

4.  Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.

Authors:  J François
Journal:  Br J Ophthalmol       Date:  1984-01       Impact factor: 4.638

5.  [Pseudoglioma in incontinentia pigmenti (author's transl)].

Authors:  W Best; F Rentsch
Journal:  Klin Monbl Augenheilkd       Date:  1974-01       Impact factor: 0.700

6.  Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family.

Authors:  A Spallone
Journal:  Br J Ophthalmol       Date:  1987-08       Impact factor: 4.638

7.  Ocular findings in incontinentia pigmenti.

Authors:  S I Rosenfeld; M E Smith
Journal:  Ophthalmology       Date:  1985-04       Impact factor: 12.079

8.  Retinal pigment epithelium in incontinentia pigmenti.

Authors:  O Mensheha-Manhart; M M Rodrigues; J A Shields; G M Shannon; R P Mirabelli
Journal:  Am J Ophthalmol       Date:  1975-04       Impact factor: 5.258

9.  Retinal and other manifestations of incontinentia pigmenti (Bloch-Sulzberger syndrome).

Authors:  M F Goldberg; P H Custis
Journal:  Ophthalmology       Date:  1993-11       Impact factor: 12.079

10.  Incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report and review of the ocular pathological features.

Authors:  J G Heathcote; B A Schoales; N R Willis
Journal:  Can J Ophthalmol       Date:  1991-06       Impact factor: 1.882

  10 in total
  6 in total

1.  ASSESSMENT OF THE RETINAL STRUCTURE IN CHILDREN WITH INCONTINENTIA PIGMENTI.

Authors:  Shwetha Mangalesh; Xi Chen; Du Tran-Viet; Christian Viehland; Sharon F Freedman; Cynthia A Toth
Journal:  Retina       Date:  2017-08       Impact factor: 4.256

2.  Macular vasculopathy and its evolution in incontinentia pigmenti.

Authors:  M F Goldberg
Journal:  Trans Am Ophthalmol Soc       Date:  1998

3.  Multimodal Retinal Imaging in Incontinentia Pigmenti Including Optical Coherence Tomography Angiography: Findings From an Older Cohort With Mild Phenotype.

Authors:  Tin Yan Alvin Liu; Ian C Han; Morton F Goldberg; Marguerite O Linz; Connie J Chen; Adrienne W Scott
Journal:  JAMA Ophthalmol       Date:  2018-05-01       Impact factor: 7.389

4.  Preliminary ocular histopathological observations on heterozygous NEMO-deficient mice.

Authors:  Stephen F Oster; D Scott McLeod; T Otsuji; Morton F Goldberg; Gerard A Lutty
Journal:  Exp Eye Res       Date:  2008-11-24       Impact factor: 3.467

5.  Child with a mild phenotype of Incontinentia Pigmenti and inner retinal dysfunction.

Authors:  Ana Maria Cunha; Jorge Breda; Amândio Rocha-Sousa; Fernando Falcão-Reis; Renato Santos-Silva
Journal:  Doc Ophthalmol       Date:  2021-02-13       Impact factor: 2.379

6.  Incontinentia pigmenti in a child with suspected retinoblastoma.

Authors:  Stephanie J Weiss; Archana Srinivasan; Michael A Klufas; Carol L Shields
Journal:  Int J Retina Vitreous       Date:  2017-09-18
  6 in total

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