Dermatopathia pigmentosa reticularis has an autosomal dominant pattern of inheritance
Specialty
Medical genetics
Dermatopathia pigmentosa reticularis(DPR) is a rare, autosomal dominant[2] congenital disorder that is a form of ectodermal dysplasia. Dermatopathia pigmentosa reticularis is composed of the triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.[3]: 856 DPR is a non life-threatening disease that largely affects the skin, hair, and nails.[4] It has also been identified as a keratin disorder.[5] Historically, as of 1992, only 10 cases had been described in world literature; however, due to recent advances in genetic analysis, five additional families studied in 2006 have been added to the short list of confirmed cases.[2][5]
^Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
^ abHeimer WL II, Brauner G, James WD (1992). "Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheritance". J Am Acad Dermatol. 26 (2 pt. 2): 298–301. doi:10.1016/0190-9622(92)70039-I. PMID 1303619.
^James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
^Heimer, W. L.; Brauner, G.; James, W. D. (February 1992). "Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheritance". Journal of the American Academy of Dermatology. 26 (2 Pt 2): 298–301. doi:10.1016/0190-9622(92)70039-i. ISSN 0190-9622. PMID 1303619.
^ abCite error: The named reference pmid16960809 was invoked but never defined (see the help page).
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