Large congenital atypical café-au-lait macules suggest superimposed mosaicism in NF1

Comment

. 2021 Jun;19(6):912-914.

doi: 10.1111/ddg.14551_g.

[Article in German]

Comment

[Article in German]

Max Görg. J Dtsch Dermatol Ges. 2021 Jun.

. 2021 Jun;19(6):912-914.

doi: 10.1111/ddg.14551_g.

No abstract available

Comment on

Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancy.
García-Martínez FJ, Azorín D, Duat-Rodríguez A, Hernández-Martín Á. García-Martínez FJ, et al. J Dtsch Dermatol Ges. 2021 Jan;19(1):73-80. doi: 10.1111/ddg.14322. Epub 2021 Jan 14. J Dtsch Dermatol Ges. 2021. PMID: 33448128

[McCune-Albright syndrome revealed by Blaschko-linear café-au-lait spots on the back].
Jung AJ, Soskin S, Paris F, Lipsker D. Jung AJ, et al. Ann Dermatol Venereol. 2016 Jan;143(1):21-6. doi: 10.1016/j.annder.2015.10.585. Epub 2015 Nov 25. Ann Dermatol Venereol. 2016. PMID: 26610360 French.
A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.
Morava E, Bartsch O, Czako M, Frensel A, Kárteszi J, Kosztolányi GY. Morava E, et al. Genet Couns. 2003;14(3):337-42. Genet Couns. 2003. PMID: 14577679
Genetic analyses of mosaic neurofibromatosis type 1 with giant café-au-lait macule, plexiform neurofibroma and multiple melanocytic nevi.
Hida T, Idogawa M, Okura M, Sugita S, Sugawara T, Sasaki Y, Tokino T, Yamashita T, Uhara H. Hida T, et al. J Dermatol. 2020 Jun;47(6):658-662. doi: 10.1111/1346-8138.15327. Epub 2020 Apr 4. J Dermatol. 2020. PMID: 32246533
Bilateral segmental neurofibromatosis: a case report and review.
Gonzalez G, Russi ME, Lodeiros A. Gonzalez G, et al. Pediatr Neurol. 2007 Jan;36(1):51-3. doi: 10.1016/j.pediatrneurol.2006.07.011. Pediatr Neurol. 2007. PMID: 17162198 Review.
Multiple café au lait spots in familial patients with MAP2K2 mutation.
Takenouchi T, Shimizu A, Torii C, Kosaki R, Takahashi T, Saya H, Kosaki K. Takenouchi T, et al. Am J Med Genet A. 2014 Feb;164A(2):392-6. doi: 10.1002/ajmg.a.36288. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311457 Review.