Literature DB >> 567211

[Genetic interpretation of linear skin abnormalities].

R Happle.   

Abstract

For the linear distribution of congenital skin lesions, modern genetics offers several explanations. Localized linear nevi may be due to somatic mutations. Generalized linear nevi may be the result of early somatic mutations or of gametic half chromatid mutations. The generalized linear patterns of incontinentia pigmenti, focal dermal hypoplasia and sex-linked chondrodysplasia punctata may be explained by functional X-chromosome mosaicism. The same mechanism may account for a peculiar striation of bones observed in focal dermal hypoplasia. Exceptional cases of incontinentia pigmenti and focal dermal hypoplasia in males may be due in part to the gonosome constitution XXY, and in part to gametic half chromatid mutations.

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Year:  1978        PMID: 567211

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  4 in total

1.  X-linked dominant chondrodysplasia punctata. Review of literature and report of a case.

Authors:  R Happle
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  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

3.  Epidermal mosaicism and Blaschko's lines.

Authors:  C Moss; S Larkins; M Stacey; A Blight; P A Farndon; E V Davison
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

4.  Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.

Authors:  Birsen Karaman; Hülya Kayserili; Asadollah Ghanbari; Zehra Oya Uyguner; Güven Toksoy; Umut Altunoglu; Seher Basaran
Journal:  Mol Cytogenet       Date:  2018-08-17       Impact factor: 2.009

  4 in total

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