Literature DB >> 14994228

Melorheostosis may originate as a type 2 segmental manifestation of osteopoikilosis.

Rudolf Happle1.   

Abstract

Melorheostosis is a non-hereditary disorder involving the bones in a segmental pattern, whereas osteopoikilosis is a rather mild disseminated bone disorder inherited as an autosomal dominant trait. Interestingly, melorheostosis and osteopoikilosis may sometimes occur together. In analogy to various autosomal dominant skin disorders for which a type 2 segmental manifestation has been postulated, melorheostosis may be best explained in such cases as a type 2 segmental osteopoikilosis, resulting from early loss of the corresponding wild type allele at the gene locus of this autosomal dominant bone disorder. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14994228     DOI: 10.1002/ajmg.a.20454

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 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

2.  [(Over-)flowing bone: the rare disease of melorheostosis: clinical presentation and therapeutic concepts demonstrated by three cases].

Authors:  E Hesse; J Brand; L Bastian; C Krettek; R Meller
Journal:  Unfallchirurg       Date:  2008-07       Impact factor: 1.000

3.  Incidentally diagnosed melorheostosis of upper limb: case report.

Authors:  Vaclav Vyskocil; Karel Koudela; Tomas Pavelka; Kristyna Stajdlova; David Suchy
Journal:  BMC Musculoskelet Disord       Date:  2015-01-31       Impact factor: 2.362

  3 in total

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