Literature DB >> 2204043

Progressive diaphyseal dysplasia: case report and literature review.

P Aggarwal1, J P Wali, S K Sharma.   

Abstract

We describe a case of progressive diaphyseal dysplasia occurring sporadically in a 25-year-old woman. This patient had menorrhagia, and severe anemia and hepatosplenomegaly, unusual clinical features of this disease.

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Year:  1990        PMID： 2204043     DOI： 10.3928/0147-7447-19900801-14

Source DB:  PubMed          Journal:  Orthopedics        ISSN： 0147-7447            Impact factor:   1.390


  3 in total

1.  Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.

Authors:  Michael P Whyte; William G Totty; Deborah V Novack; Xiafang Zhang; Deborah Wenkert; Steven Mumm
Journal:  J Bone Miner Res       Date:  2011-05       Impact factor: 6.741

Review 2.  Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.

Authors:  R K Mondal; B Karmakar; P K Chandra; K Mukherjee
Journal:  Indian J Pediatr       Date:  2007-03       Impact factor: 5.319

3.  Seropositive Rheumatoid Arthritis with Very Unusual X-ray Findings.

Authors:  Laith Alamlih; Mohamed Alkahlout; Abdulrahim Siam; Syed Alam; Abdul-Wahab Al-Allaf
Journal:  Eur J Case Rep Intern Med       Date:  2018-07-26
  3 in total

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