Literature DB >> 788770

The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin.

R Jackson.   

Abstract

Blaschko's lines are the pattern assumed by many different naevoid and acquired skin diseases on the human skin and mucosae. They were described and drawn by Blaschko 75 years ago. These lines are to be distinguished from other linear patterns such as Voight's lines, Langer's lines, and the lines of innervation of the spinal nerves. They do not follow any known nervous, vascular or lymphatic structures in the skin. The epidermis and its appendageal structures, the melanocytes, the vascular system, and the fatty hypoderm, all, separately or in combination, may be involved in the morphological manifestations which follow Blaschko's lines. Many of the naevoid skin conditions are lifelong (e.g. linear sebaceous naevus, unilateral naevoid telangiectasia); many of the acquired skin diseases (e.g. lichen striatus, linear psoriasis) are of relatively short duration (e.g. 1-2 years). The cause of the distribution pattern is unknown. It is possibly a form of human 'mosaicism' where certain specific cells or groups of cells react differently from other cells due to chromosomal abnormalities. The embryological explanation of Blaschko's lines is not at all clear. Other markers in addition to the skin findings are needed to determine the time and the nature of the change responsible for these lines. The main purpose of this article is to introduce the concept of Blaschko's lines into the medical, paramedical, and general biological fields of science. In this way, it is hoped that some inter-reaction can occur between those who regularly see Blaschko's lines and those who regularly see and study other chromosomal and embryological abnormalities.

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Year:  1976        PMID: 788770     DOI: 10.1111/j.1365-2133.1976.tb00835.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  23 in total

1.  Localization of sclerotic-type chronic graft-vs-host disease to sites of skin injury: potential insight into the mechanism of isomorphic and isotopic responses.

Authors:  Kathryn J Martires; Kristin Baird; Deborah E Citrin; Fran T Hakim; Steven Z Pavletic; Edward W Cowen
Journal:  Arch Dermatol       Date:  2011-09

2.  Linear scleroderma en coup de sabre affecting the upper eyelid and lashes.

Authors:  Katrina A Mears; J Javier Servat; Evan H Black
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2012-01-17       Impact factor: 3.117

Review 3.  Distinct mechanisms underlie pattern formation in the skin and skin appendages.

Authors:  Randall B Widelitz; Ruth E Baker; Maksim Plikus; Chih-Min Lin; Philip K Maini; Ralf Paus; Cheng Ming Chuong
Journal:  Birth Defects Res C Embryo Today       Date:  2006-09

Review 4.  X chromosome inactivation and female predisposition to autoimmunity.

Authors:  Tayfun Ozcelik
Journal:  Clin Rev Allergy Immunol       Date:  2008-06       Impact factor: 8.667

5.  Historical outline of attempts to classify skin diseases.

Authors:  R Jackson
Journal:  Can Med Assoc J       Date:  1977-05-21       Impact factor: 8.262

6.  A case of incontinentia pigmenti associated with multiorgan abnormalities.

Authors:  Woon-Kyong Chung; Deok-Woo Lee; Sung-Eun Chang; Mi-Woo Lee; Jee-Ho Choi; Kee-Chan Moon
Journal:  Ann Dermatol       Date:  2009-02-28       Impact factor: 1.444

Review 7.  Lyonization and the lines of Blaschko.

Authors:  R Happle
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 8.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Authors:  I T Thomas; J L Frias; E S Cantu; C Z Lafer; D B Flannery; J G Graham
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

9.  Linkage and segregation analysis of black and brindle coat color in domestic dogs.

Authors:  Julie A Kerns; Edward J Cargill; Leigh Anne Clark; Sophie I Candille; Tom G Berryere; Michael Olivier; George Lust; Rory J Todhunter; Sheila M Schmutz; Keith E Murphy; Gregory S Barsh
Journal:  Genetics       Date:  2007-05-04       Impact factor: 4.562

10.  Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

Authors:  D Donnai; A P Read; C McKeown; T Andrews
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

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