Inherited patterned lentiginosis in black persons

Inherited patterned lentiginosis
Inherited patterned lentiginosis
Other names	Familial lentigines profusa
	Autosomal dominant is the inheritance manner of this condition
Specialty	Dermatology

Inherited patterned lentiginosis is an inherited skin condition that results in widespread small, flat areas of more-pigmented skin with clearly defined borders, generally noticed when the affected person is an infant or young child.^[1] The inheritance pattern is autosomal dominant,^[2]^: 686 and organs other than the skin are not affected; therefore, it is distinct from Carney complex.^[1]^[3]

References

^ ^a ^b Online Mendelian Inheritance in Man (OMIM): Inherited Patterned Lentiginosis - 151001
^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
^ Xing, Qinghe; Chen, Xiangdong; Wang, Mingtai; Bai, Wenjie; Peng, Xin; Gao, Rui; Wu, Shengnan; Qian, Xueqing; Qin, Wei (July 2005). "A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3". Human Genetics. 117 (2–3): 154–159. doi:10.1007/s00439-005-1284-1. ISSN 0340-6717. PMID 15841387.

External links

This Genodermatoses article is a stub. You can help Wikipedia by expanding it.

Zdroj:https://en.wikipedia.org?pojem=Inherited_patterned_lentiginosis_in_black_persons
Text je dostupný za podmienok Creative Commons Attribution/Share-Alike License 3.0 Unported; prípadne za ďalších podmienok. Podrobnejšie informácie nájdete na stránke Podmienky použitia.

[omim151001-1] Online Mendelian Inheritance in Man (OMIM): Inherited Patterned Lentiginosis - 151001

[Andrews-2] James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.

[3] Xing, Qinghe; Chen, Xiangdong; Wang, Mingtai; Bai, Wenjie; Peng, Xin; Gao, Rui; Wu, Shengnan; Qian, Xueqing; Qin, Wei (July 2005). "A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3". Human Genetics. 117 (2–3): 154–159. doi:10.1007/s00439-005-1284-1. ISSN 0340-6717. PMID 15841387.

[1]

[2]

[3]

Classification	D ICD-10: L81.4 OMIM: 151001
External resources	Orphanet: 231040