Familial multiple lentigines syndrome without systemic involvement[1]
Generalized lentiginosis is inherited in an autosomal dominant manner
Specialty
Dermatology
Generalized lentiginosis is a cutaneous condition that will occasionally present without other associated abnormalities.[2]: 686 It may be caused by carney complex, Noonan syndrome with multiple lentigines or Peutz–Jeghers syndrome.
^RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Familial generalized lentiginosis". www.orpha.net. Retrieved 20 April 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
^James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
and 6 Related for: Generalized lentiginosis information
Generalizedlentiginosis is a cutaneous condition that will occasionally present without other associated abnormalities.: 686 It may be caused by carney...
Torso of thirty-seven-year-old, second-generation patient, exhibiting lentiginosis. In the two predominant mutations of NSML (Y279C and T468M) the mutations...
Shengnan; Qian, Xueqing; Qin, Wei (July 2005). "A locus for familial generalizedlentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3"....
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