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Case Reports
. 2015 Jan;35(1):178-80.
doi: 10.3343/alm.2015.35.1.178. Epub 2014 Dec 8.

Identification of somatic KRAS mutation in a Korean baby with nevus sebaceus syndrome

Affiliations
Case Reports

Identification of somatic KRAS mutation in a Korean baby with nevus sebaceus syndrome

Sung Woo Kim et al. Ann Lab Med. 2015 Jan.
No abstract available

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Conflict of interest statement

No potential conflicts of interest to this article were reported.

Figures

Fig. 1
Fig. 1
Clinical features of nevus sebaceus. (A) Well-demarcated slippery, skin-colored, orange-peel like, linear plaque on the patient's left parietal scalp and face. (B) Round plaque on the patient's occipital scalp, showing alopecia. (C) A limbal dermoid with a skin-colored pedunculated papule on the left eyelid.
Fig. 2
Fig. 2
Pathology of nevus sebaceus showing proliferative changes of sebaceous glands and apocrine glands in the epidermis (H&E, ×100).
Fig. 3
Fig. 3
The KRAS mutation (c.35G>A; p.Gly12Asp) was identified in genomic DNA isolated from the nevus sebaceus lesion (arrows), but not from adjacent normal skin tissue or peripheral blood leukocytes.

References

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