Br J Ophthalmol. 1984 Jan;68(1):19-25.

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

Abstract

Incontinentia pigmenti is associated with various anomalies in 80% of cases. Among the most important are the ocular abnormalities and more particularly a retrolental mass with detachment of a dysplastic retina. At the basis of this manifestation are retinal vascular changes, characterised at first by ectatic tortuous veins and arteriovenous anastomoses as well as by aneurysmal-like dilatations.

PMID:: 6689930; [PubMed - indexed for MEDLINE]
PMCID:: PMC1040231

Free PMC Article

Publication Types, MeSH Terms

Publication Types

Case Reports

MeSH Terms

LinkOut - more resources

Full Text Sources

Medical

Skin Pigmentation Disorders - MedlinePlus Health Information

Supplemental Content

Save items

Related citations in PubMed

Fundus changes in incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report. [Br J Ophthalmol. 1978]
Fundus changes in incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.
Jain RB, Willetts GS. Br J Ophthalmol. 1978 Sep; 62(9):622-6.
Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family. [Br J Ophthalmol. 1987]
Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family.
Spallone A. Br J Ophthalmol. 1987 Aug; 71(8):629-34.
Incontinentia pigmenti. A world statistical analysis. [Arch Dermatol. 1976]
Incontinentia pigmenti. A world statistical analysis.
Carney RG. Arch Dermatol. 1976 Apr; 112(4):535-42.
Review Incontinentia pigmenti: a review. [Cutis. 1988]
Review Incontinentia pigmenti: a review.
el-Benhawi MO, George WM. Cutis. 1988 Apr; 41(4):259-62.
Review Incontinentia pigmenti (Bloch-Sulzberger syndrome). [J Med Genet. 1993]
Review Incontinentia pigmenti (Bloch-Sulzberger syndrome).
Landy SJ, Donnai D. J Med Genet. 1993 Jan; 30(1):53-9.

See reviews... See all...

Cited by 6 PubMed Central articles

Persistent Fetal Vasculature and Severe Protein C Deficiency. [Mol Syndromol. 2010]
Persistent Fetal Vasculature and Severe Protein C Deficiency.
Douglas AG, Rafferty H, Hodgkins P, Nagra A, Foulds NC, Morgan M, Temple IK. Mol Syndromol. 2010; 1(2):82-86. Epub 2010 Apr 23.
Novel corneal features in two males with incontinentia pigmenti. [Br J Ophthalmol. 2003]
Novel corneal features in two males with incontinentia pigmenti.
Mayer EJ, Shuttleworth GN, Greenhalgh KL, Sansom JE, Grey RH, Kenwrick S. Br J Ophthalmol. 2003 May; 87(5):554-6.
Review Incontinentia pigmenti (Bloch-Sulzberger syndrome). [J Med Genet. 1993]
Review Incontinentia pigmenti (Bloch-Sulzberger syndrome).
Landy SJ, Donnai D. J Med Genet. 1993 Jan; 30(1):53-9.

See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Compound
PubChem chemical compound records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records. Multiple substance records may contribute to the PubChem compound record.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
References for this PMC Article
Citation referenced in PubMed article. Only valid for PubMed citations that are also in PMC.
Substance
PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.
Free in PMC
Free full text articles in PMC
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.
Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes.
Br J Ophthalmol. 1984 Jan ;68(1):19-25.

PubMed
Hemoglobin Presbyterian: beta108 (G10) asparagine leads to lysine, A hemoglobin ...
Hemoglobin Presbyterian: beta108 (G10) asparagine leads to lysine, A hemoglobin variant with low oxygen affinity.
FEBS Lett. 1978 Aug 1 ;92(1):53-6.

PubMed
Deduced amino acid sequence from the bovine oxytocin-neurophysin I precursor cDN...
Deduced amino acid sequence from the bovine oxytocin-neurophysin I precursor cDNA.
Nature. 1983 Mar 24-30 ;302(5906):342-4.

PubMed
Tubular adenoma of breast.
Tubular adenoma of breast.
Arch Pathol Lab Med. 1983 Feb ;107(2):84-6.

PubMed
Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-...
Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids.
Eur J Pediatr. 1978 Jul 19 ;128(4):225-33.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to: