Literature DB >> 18429779

Phacomatosis pigmentovascularis type Va in a 3-month old.

Margarita Larralde1, Andrea Santos-Muñoz, María Rodríguez Cáceres, Analía Ciardiullo.   

Abstract

Phacomatosis pigmentovascularis is a rare genodermatosis characterized by a combination of melanocytic nevi and vascular malformations. A new type of phacomatosis pigmentovascularis was recently described which included cutis marmorata telangiectatica congenita and aberrant Mongolian spots and was named type V. We report a 3-month-old girl with diagnosis of phacomatosis pigmentovascularis type V.

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Year:  2008        PMID： 18429779     DOI： 10.1111/j.1525-1470.2008.00633.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN： 0736-8046            Impact factor:   1.588


  4 in total

Review 1.  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

2.  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

3.  Mongolian spots: How important are they?

Authors:  Divya Gupta; Devinder Mohan Thappa
Journal:  World J Clin Cases       Date:  2013-11-16       Impact factor: 1.337

4.  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
  4 in total

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