Literature DB >> 507873

Linear melorheostotic scleroderma with hypertrichosis.

Y Miyachi, T Horio, A Yamada, T Ueo.   

Abstract

On the basis of clinical features and histological findings, cutaneous manifestations of linear melorheostotic scleroderma are apparently derived from a localized proliferative disorder and are not secondary to bone changes. If the hypertrichosis has the same origin as the osteocutaneous changes, melorheostosis may represent a congenital disorder with both ectodermic and mesodermic components.

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Mesh:

Year:  1979        PMID: 507873

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  4 in total

1.  Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS.

Authors:  Michael P Whyte; Malachi Griffith; Lee Trani; Steven Mumm; Gary S Gottesman; William H McAlister; Kilannin Krysiak; Robert Lesurf; Zachary L Skidmore; Katie M Campbell; Ilana S Rosman; Susan Bayliss; Vinieth N Bijanki; Angela Nenninger; Brian A Van Tine; Obi L Griffith; Elaine R Mardis
Journal:  Bone       Date:  2017-04-21       Impact factor: 4.398

Review 2.  Linear scleroderma and melorheostosis: case presentation and literature review.

Authors:  M J Moreno Alvarez; M A Lázaro; G Espada; H A Barceló; A Maldonado Cocco
Journal:  Clin Rheumatol       Date:  1996-07       Impact factor: 2.980

3.  Unilateral nevoid telangiectasia associated with ipsilateral melorheostosis.

Authors:  Jihyun Kim; Sung Bin Cho; Suhyun Cho; Dongsik Bang
Journal:  Ann Dermatol       Date:  2012-04-26       Impact factor: 1.444

4.  Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant.

Authors:  Benjamin Korman; Jun Wei; Anne Laumann; Polly Ferguson; John Varga
Journal:  Case Rep Dermatol Med       Date:  2016-06-13
  4 in total

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