Familial progressive hyperpigmentation: Difference between revisions
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{{Infobox medical condition (new) |
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| ⚫ | '''Familial progressive hyperpigmentation''' is characterized by patches of hyperpigmentation, present at birth, which increase in size and number with age.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN |
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| name = Familial progressive hyperpigmentation |
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| synonyms = Melanosis universalis hereditaria<ref>{{cite web |last1=RESERVED |first1=INSERM US14-- ALL RIGHTS |title=Orphanet: Familial progressive hyperpigmentation |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79146 |website=www.orpha.net |access-date=20 April 2019 |language=en}}</ref> |
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| image = Autosomal dominant - en.svg |
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| caption = This condition in inherited in an autosomal dominant manner |
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| field = [[Medical genetics]] |
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| ⚫ | '''Familial progressive hyperpigmentation''' is characterized by patches of [[hyperpigmentation]], present at birth, which increase in size and number with age. This is a [[Genetic disorder|genetic disease]], however the [[gene]] that accounts for this spotty darkening of the skin has yet to be discovered. Although rare, the [[Congenital disorder|congenital disease]] is most prevalent among populations originating from [[China]].<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}.</ref>{{rp|858}} |
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==See also== |
==See also== |
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==References== |
==References== |
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The American Journal of Human Genetics 84, 672–677, May 15, 2009 |
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== External links == |
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{{Medical resources |
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| ICD10 = L81.4 |
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| ICD9 = <!--{{ICD9|xxx}}--> |
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| OMIM = 145250 |
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| Orphanet = 79146 |
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{{Pigmentation disorders}} |
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{{Dermatology-stub}} |
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[[Category:Disturbances of human pigmentation]] |
[[Category:Disturbances of human pigmentation]] |
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{{Genodermatoses-stub}} |
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Latest revision as of 00:38, 6 May 2024
| Familial progressive hyperpigmentation | |
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| Other names | Melanosis universalis hereditaria[1] |
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| This condition in inherited in an autosomal dominant manner | |
| Specialty | Medical genetics |
Familial progressive hyperpigmentation is characterized by patches of hyperpigmentation, present at birth, which increase in size and number with age. This is a genetic disease, however the gene that accounts for this spotty darkening of the skin has yet to be discovered. Although rare, the congenital disease is most prevalent among populations originating from China.[2]: 858
See also
[edit]References
[edit]- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Familial progressive hyperpigmentation". www.orpha.net. Retrieved 20 April 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
The American Journal of Human Genetics 84, 672–677, May 15, 2009