Literature DB >> 17512229

A case of Sturge-Weber syndrome in association with phacomatosis pigmentovascularis and developmental glaucoma.

Archana Gupta1, Suneeta Dubey, Manisha Agarwal.   

Abstract

Sturge-Weber syndrome is a rare neurocutaneous disorder characterized by a facial nevus flammeus and extensive angiomatous changes involving the leptomeninges, the dura, and vessels of the gray and white matter. Oculodermal melanocytosis is characterized by hyperpigmentation of the facial skin in the distribution of the ophthalmic, maxillary, and occasionally mandibular division of the trigeminal nerve.

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Year:  2007        PMID： 17512229     DOI： 10.1016/j.jaapos.2007.02.016

Source DB:  PubMed          Journal:  J AAPOS        ISSN： 1091-8531            Impact factor:   1.220


  3 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.  Bilateral Sturge-Weber and Phakomatosis Pigmentovascularis with Glaucoma, an Overlap Syndrome.

Authors:  Bharat Patil; Gautam Sinha; Bhagabat Nayak; Reetika Sharma; Sadhana Kumari; Tanuj Dada
Journal:  Case Rep Ophthalmol Med       Date:  2015-05-06

3.  Phakomatosis pigmentovascularis presenting with sturge-weber syndrome and klippel-trenaunay syndrome.

Authors:  Sumit Sen; Sanchaita Bala; Chinmay Halder; Rahul Ahar; Anusree Gangopadhyay
Journal:  Indian J Dermatol       Date:  2015 Jan-Feb       Impact factor: 1.494
  3 in total

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