Literature DB >> 12588390

Cutis marmorata telangiectatica congenita and extensive mongolian spots: type 5 phacomatosis pigmentovascularis.

A Torrelo1, A Zambrano, R Happle.   

Abstract

Two patients with an unusual association of extensive cutis marmorata telangiectatica congenita and aberrant mongolian spots are reported. We believe that such association is best explained as a phenomenon of non-allelic twin spotting. We found only one previous similar case in a textbook, and we support the classification of this condition as phacomatosis pigmentovascularis type V.

Entities:  

Mesh：

Year:  2003        PMID： 12588390     DOI： 10.1046/j.1365-2133.2003.05118.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


  12 in total

1.  A Neonatal Case of Phacomatosis Pigmentovascularis Type IIa.

Authors:  Ezgi Ünlü; Tijen Şahin
Journal:  Balkan Med J       Date:  2015-01-01       Impact factor: 2.021

2.  The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.

Authors:  Han Ma; Mengsi Liao; Shu Qiu; Ruijun Luo; Rongbiao Lu; Chun Lu
Journal:  An Bras Dermatol       Date:  2015 May-Jun       Impact factor: 1.896

Review 3.  Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.

Authors:  Akash Kumar; Diane B Zastrow; Elijah J Kravets; Daniah Beleford; Maura R Z Ruzhnikov; Megan E Grove; Annika M Dries; Jennefer N Kohler; Daryl M Waggott; Yaping Yang; Yong Huang; Katherine M Mackenzie; Christine M Eng; Paul G Fisher; Euan A Ashley; Joyce M Teng; David A Stevenson; Joseph T Shieh; Matthew T Wheeler; Jonathan A Bernstein
Journal:  Am J Med Genet A       Date:  2019-03-28       Impact factor: 2.802

4.  Phacomatosis Pigmentovascularis Type Vb in a Three-Year Old Boy.

Authors:  Hee Jin Jun; So Min Kim; Sang Hyun Cho; Jeong Deuk Lee; Hei Sung Kim
Journal:  Ann Dermatol       Date:  2015-05-29       Impact factor: 1.444

5.  ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.

Authors:  Iman S Abumansour; Hadia Hijazi; Anas Alazmi; Fatma Alzahrani; Fahad A Bashiri; Hamdy Hassan; Mohammed Alhaddab; Fowzan S Alkuraya
Journal:  Hum Genet       Date:  2015-05-10       Impact factor: 4.132

6.  Phacomatosis pigmentovascularis type IIa--case report.

Authors:  Majoriê Mergen Segatto; Eloísa Unfer Schmitt; Laura Netto Hagemann; Roberta Castilhos da Silva; Cristiane Almeida Soares Cattani
Journal:  An Bras Dermatol       Date:  2013 Nov-Dec       Impact factor: 1.896

7.  Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital Glaucoma.

Authors:  Yangfan Yang; Xiujuan Guo; Jiangang Xu; Yiming Ye; Xiaoan Liu; Minbin Yu
Journal:  Medicine (Baltimore)       Date:  2015-07       Impact factor: 1.889

8.  Cutis marmorata telangiectatica congenita and aberrant Mongolian spots: Type V phacomatosis pigmentovascularis or phacomatosis cesiomarmorata.

Authors:  Guilian Du; Xiaomin Zhang; Tangde Zhang
Journal:  JAAD Case Rep       Date:  2016-01-23

9.  Laser therapy treatment of phacomatosis pigmentovascularis type II: two case reports.

Authors:  Koji Adachi; Shinji Togashi; Kaoru Sasaki; Mitsuru Sekido
Journal:  J Med Case Rep       Date:  2013-02-27

10.  Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association.

Authors:  Anubhav Garg; Lalit K Gupta; A K Khare; C M Kuldeep; Asit Mittal; Sharad Mehta
Journal:  Indian Dermatol Online J       Date:  2013-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.