Literature DB >> 10398255

Extracutaneous analogies of Blaschko lines.

H D Rott1.   

Abstract

In females, early random X-chromosome inactivation in the late blastocyst and subsequent embryonic development cause a random distribution of cells with an active paternal or maternal X-chromosome. Carriers of X-linked disorders are mostly healthy but, when thoroughly examined, may display a characteristic pattern of partial involvement, which for the skin, is known to follow the lines of Blaschko. Comparable patterns of involvement have been seen in various other organs. The evaluation of carriers who are heterozygous for X-linked disorders, therefore, is an efficient method for the study of functional genetic mosaicism in humans. The same patterns can also be seen in case of early embryonic somatic mutations. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10398255     DOI: 10.1002/(sici)1096-8628(19990806)85:4<338::aid-ajmg5>3.0.co;2-8

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Ophthalmological manifestations in segmental neurofibromatosis type 1.

Authors:  M Ruggieri; P Pavone; A Polizzi; M Di Pietro; A Scuderi; A Gabriele; A Spalice; P Iannetti
Journal:  Br J Ophthalmol       Date:  2004-11       Impact factor: 4.638

2.  Oral HRAS Mutation in Orofacial Nevus Sebaceous Syndrome (Schimmelpenning-Feuerstein-Mims-Syndrome): A Case Report With a Literature Survey.

Authors:  Reinhard E Friedrich; Martin Gosau; Andreas M Luebke; Christian Hagel; Felix K Kohlrusch; Michael Hahn; Simon VON Kroge; Jan Hahn; Ilse Wieland; Martin Zenker
Journal:  In Vivo       Date:  2022 Jan-Feb       Impact factor: 2.155

3.  Pulmonary hypertension and vasculopathy in incontinentia pigmenti: a case report.

Authors:  Abduljabbar Alshenqiti; Marwan Nashabat; Hissah AlGhoraibi; Omar Tamimi; Majid Alfadhel
Journal:  Ther Clin Risk Manag       Date:  2017-05-09       Impact factor: 2.423

  3 in total

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