Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Nov 4:31:59-61.
doi: 10.1016/j.jdcr.2022.10.030. eCollection 2023 Jan.

Extensive blaschkoid macules and patches since birth

Affiliations

Extensive blaschkoid macules and patches since birth

Suzanne Xu et al. JAAD Case Rep. .
No abstract available

Keywords: Blaschko’s lines; FDH, focal dermal hypoplasia; Goltz syndrome; LWNH, linear and whorled nevoid hypermelanosis; MLS, microphthalmia with linear skin defects syndrome; RTS, Rothmund-Thomson syndrome; X-linked dominant disorder; focal dermal hypoplasia.

PubMed Disclaimer

Conflict of interest statement

None disclosed.

Figures

Fig 1
Fig 1
Fig 2
Fig 2
Fig 3
Fig 3

Similar articles

Cited by

References

    1. Aravind M., Do T.T., Cha H.C., Fullen D.R., Cha K.B. Blaschkolinear acquired inflammatory skin eruption, or blaschkitis, with features of lichen nitidus. JAAD Case Rep. 2016;2(2):102–104. doi: 10.1016/j.jdcr.2015.12.008. - DOI - PMC - PubMed
    1. Temple I.K., MacDowall P., Baraitser M., Atherton D.J. Focal dermal hypoplasia (Goltz syndrome) J Med Genet. Mar 1990;27(3):180–187. doi: 10.1136/jmg.27.3.180. - DOI - PMC - PubMed
    1. Hafsi W., Toukabri N., Souissi A., et al. In: Atlas of dermatology, dermatopathology and venereology. Smoller B., Bagherani N., editors. Springer International Publishing; 2020. Genodermatoses; pp. 1–28.
    1. Di Lernia V. Linear and whorled hypermelanosis. Pediatr Dermatol. 2007;24(3):205–210. doi: 10.1111/j.1525-1470.2007.00387.x. - DOI - PubMed
    1. Harmsen M.-B., Azzarello-Burri S., García González M.M., et al. Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. Eur J Hum Genet. 2009;17(10):1207–1215. doi: 10.1038/ejhg.2009.40. - DOI - PMC - PubMed

LinkOut - more resources