Generalized lentiginosis
{{Infobox medical condition (new)
| name = Generalized lentiginosis
| synonyms = Familial multiple lentigines syndrome without systemic involvement{{cite web |last1=RESERVED |first1=INSERM US14-- ALL RIGHTS |title=Orphanet: Familial generalized lentiginosis |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231040 |website=www.orpha.net |access-date=20 April 2019 |language=en}}
| image = Autosomal dominant - en.svg
| image_size = 150px
| caption = Generalized lentiginosis is inherited in an autosomal dominant manner
| pronounce =
| field =
| symptoms =
| complications =
| onset =
| duration =
| types =
| causes =
| risks =
| diagnosis =
| differential =
| prevention =
| treatment =
| medication =
| prognosis =
| frequency =
| deaths =
}}
Generalized lentiginosis is a cutaneous condition that will occasionally present without other associated abnormalities.{{cite book |author1=James, William D. |author2=Berger, Timothy G. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |year=2006 |isbn=0-7216-2921-0 |display-authors=etal}}{{rp|686}} It may be caused by carney complex, Noonan syndrome with multiple lentigines or Peutz–Jeghers syndrome.
See also
References
{{reflist}}
External links
{{Medical resources
| DiseasesDB =
| ICD10 = L81.4 (ILDS L81.406)
| ICD9 =
| ICDO =
| OMIM = 151001
| MedlinePlus =
| eMedicineSubj =
| eMedicineTopic =
| MeshID =
| Orphanet = 231040
}}
{{Pigmentation disorders}}
Category:Melanocytic nevi and neoplasms
{{Cutaneous-condition-stub}}