Literature DB >> 18210039

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

E Hesse1, J Brand, L Bastian, C Krettek, R Meller.   

Abstract

Melorheostosis is a rare, benign, and sporadically occurring osteosclerosis of unknown cause. The onset of the disease is usually in early adulthood. Melorheostosis affects both genders, develops progressively, and is usually limited to one side of the human body. The sclerosis originates predominantly from the cortices of the long bones of the lower limbs and rarely the upper limbs. Frequently, the sclerosis involves the soft tissue surrounding the affected bones which may cause limitations in the range of motion, contractures, deformities, and pain. Melorheostosis is usually diagnosed by radiograms. Pain relief and restoration of the full range of motion are the primary goals of the therapeutic approach. A good outcome cannot always be achieved and a recurrence of the disease happens very often.

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Year:  2008        PMID: 18210039     DOI: 10.1007/s00113-007-1368-6

Source DB:  PubMed          Journal:  Unfallchirurg        ISSN: 0177-5537            Impact factor:   1.000


  20 in total

1.  Melorheostosis of the skeletally immature hand: a case report and long-term follow-up evaluation.

Authors:  R Rozencwaig; M R Wilson; G B McFarland
Journal:  J Hand Surg Am       Date:  1996-07       Impact factor: 2.230

2.  Melorheostosis--an unusual cause of amputation.

Authors:  L E Graham; R C Parke
Journal:  Prosthet Orthot Int       Date:  2005-04       Impact factor: 1.895

3.  Advanced imaging of melorheostosis with emphasis on MRI.

Authors:  A M Judkiewicz; M D Murphey; C S Resnik; A H Newberg; H T Temple; W S Smith
Journal:  Skeletal Radiol       Date:  2001-08       Impact factor: 2.199

4.  Melorheostosis in a patient with familial osteopoikilosis.

Authors:  C E Butkus; V V Michels; N M Lindor; W P Cooney
Journal:  Am J Med Genet       Date:  1997-10-03

5.  A case of melorheostosis with associated linear cutaneous vascular malformation.

Authors:  D R Taylor
Journal:  Clin Exp Dermatol       Date:  1981-01       Impact factor: 3.470

Review 6.  Bone dysplasia series. Melorheostosis: review and update.

Authors:  A Greenspan; E M Azouz
Journal:  Can Assoc Radiol J       Date:  1999-10       Impact factor: 2.248

7.  Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third family.

Authors:  Philippe Debeer; E Pykels; J Lammens; K Devriendt; J-P Fryns
Journal:  Am J Med Genet A       Date:  2003-06-01       Impact factor: 2.802

Review 8.  Melorheostosis may originate as a type 2 segmental manifestation of osteopoikilosis.

Authors:  Rudolf Happle
Journal:  Am J Med Genet A       Date:  2004-03-15       Impact factor: 2.802

9.  Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis.

Authors:  Jan Hellemans; Philippe Debeer; Michael Wright; Andreas Janecke; Klaus W Kjaer; Peter C M Verdonk; Ravi Savarirayan; Lina Basel; Celia Moss; Johannes Roth; Albert David; Anne De Paepe; Paul Coucke; Geert R Mortier
Journal:  Hum Mutat       Date:  2006-03       Impact factor: 4.878

10.  Melorheostosis and the sclerotomes: a radiological correlation.

Authors:  R O Murray; J McCredie
Journal:  Skeletal Radiol       Date:  1979-06-06       Impact factor: 2.199

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