Literature DB >> 3894210

Lyonization and the lines of Blaschko.

R Happle.   

Abstract

The lines of Blaschko represent a nonrandom developmental pattern of the skin fundamentally differing from the system of dermatomes. Many nevoid skin lesions display an arrangement following these lines. This is a review of case reports providing photographically documented evidence that the lines of Blaschko become manifest in the heterozygous state of various X-linked gene defects such as incontinentia pigmenti, focal dermal hypoplasia, X-linked dominant chondrodysplasia punctata, X-linked hypohidrotic ectodermal dysplasia, and Menkes syndrome. Hence, a causal relationship between lyonization and the lines of Blaschko seems quite obvious. Although it should be borne in mind that other genetic mechanisms such as somatic mutations or chimerism may give rise to the same linear pattern, the datable embryologic event of X-inactivation seems most suitable to explain the origin and nature of the lines of Blaschko. Apparently, in women affected with X-linked skin disorders the lines of Blaschko visualize the clonal proliferation of two functionally different populations of cells during early embryogenesis of the skin. The typical dorsal V-shape and the abdominal S-figure of these lines may result from an interference of the transversal coherent proliferation with the longitudinal growth and flexion of the embryo. In contrast to Blaschko's original assumption, it is now clear that these lines are independent from the metameric structure of the human body. Obviously, they represent a marker of the normal development of human skin. Therefore, a thorough study of the distribution pattern of X-linked skin disorders in women may give us a better insight into the early embryogeny of the human integument.

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Year:  1985        PMID: 3894210     DOI: 10.1007/bf00273442

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  44 in total

1.  Letter: Half chromatid mutations may explain incontinentia pigmenti in males.

Authors:  W Lenz
Journal:  Am J Hum Genet       Date:  1975-09       Impact factor: 11.025

2.  [ON A SYSTEMATIZED NEVIFORM ATROPHODERMA].

Authors:  O BRAUN-FALCO; S MARGHESCU
Journal:  Arch Klin Exp Dermatol       Date:  1965-03-24

3.  [Genetic significance of Blaschko's lines].

Authors:  R Happle
Journal:  Z Hautkr       Date:  1977-09-15

4.  A comparative study of the coats of chimaeric mice and those of heterozygotes for X-linked genes.

Authors:  B M Cattanach; H G Wolfe; M F Lyon
Journal:  Genet Res       Date:  1972-06       Impact factor: 1.588

5.  Menkes kinky hair syndrome in a black infant.

Authors:  E J Volpintesta
Journal:  Am J Dis Child       Date:  1974-08

6.  Incontinentia pigmenti: clinical and genetical studies of two familial cases.

Authors:  H Gordon; W Gordon
Journal:  Dermatologica       Date:  1970

7.  Skin manifestations of Conradi's disease. Chondrodystrophia congenita punctata.

Authors:  E L Bodian
Journal:  Arch Dermatol       Date:  1966-12

8.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Familial cutaneous amyloidosis with systemic manifestations in males.

Authors:  M W Partington; P J Marriott; R S Prentice; A Cavaglia; N E Simpson
Journal:  Am J Med Genet       Date:  1981

10.  The Bloch-Sulzberger syndrome (incontinentia pigmenti).

Authors:  H HABER
Journal:  Br J Dermatol       Date:  1952-04       Impact factor: 9.302

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  30 in total

1.  Aplasia cutis congenita reminiscent of the lines of Blaschko.

Authors:  R C Hennekam
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

2.  Deletion 3q27----3qter associated with a new skin disorder?

Authors:  R Happle
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography.

Authors:  R P Clark; M R Goff; K D MacDermot
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

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.  Somatic recombination may explain linear psoriasis.

Authors:  R Happle
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

6.  Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita.

Authors:  K Devriendt; G Matthijs; E Legius; E Schollen; D Blockmans; C van Geet; H Degreef; J J Cassiman; J P Fryns
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

Review 7.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Authors:  E Hatchwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

Review 8.  Genodermatoses caused by genetic mosaicism.

Authors:  M Vreeburg; M A M van Steensel
Journal:  Eur J Pediatr       Date:  2012-11-01       Impact factor: 3.183

Review 9.  Pathogenesis-based therapies in ichthyoses.

Authors:  Joey E Lai-Cheong; Peter M Elias; Amy S Paller
Journal:  Dermatol Ther       Date:  2013 Jan-Feb       Impact factor: 2.851

Review 10.  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

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