Literature DB >> 7917133

Camurati-Engelmann disease: contribution of bone scintigraphy to genetic counseling.

C Clybouw1, S Desmyttere, M Bonduelle, A Piepsz.   

Abstract

Progressive diaphyseal dysplasia (Camurati-Engelmann disease) is a rare hereditary disorder of bone characterized by progressive, bilaterally symmetrical diaphyseal sclerosis of the long bones. Severely affected patients show muscle weakness, waddling gait and severe pain in the extremities. However, clinical and radiological investigations in families with Camurati-Engelmann disease demonstrate a wide variability in expression of the manifestations. Asymptomatic patients were in several instances diagnosed only after radiologic screening of relatives. Although considered an autosomal dominant disorder, families are described where neither clinical nor radiological manifestations can be demonstrated in direct ancestors of patients. Combining roentgenographic examination with bone scintigraphy seems therefore necessary in confirming or ruling out progressive diaphyseal dysplasia in each family member.

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Year:  1994        PMID: 7917133

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  10 in total

1.  Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3.

Authors:  M Ghadami; Y Makita; K Yoshida; G Nishimura; Y Fukushima; K Wakui; S Ikegawa; K Yamada; S Kondo; N Niikawa; H a Tomita
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Camurati-Engelmann disease: failure of response to bisphosphonates: report of two cases.

Authors:  Glaucio R W Castro; Simone Appenzeller; João Francisco Marques-Neto; Manoel B Bértolo; Adil M Samara; Ibsen Coimbra
Journal:  Clin Rheumatol       Date:  2005-01-20       Impact factor: 2.980

Review 3.  Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment.

Authors:  K Janssens; F Vanhoenacker; M Bonduelle; L Verbruggen; L Van Maldergem; S Ralston; N Guañabens; N Migone; S Wientroub; M T Divizia; C Bergmann; C Bennett; S Simsek; S Melançon; T Cundy; W Van Hul
Journal:  J Med Genet       Date:  2005-05-13       Impact factor: 6.318

Review 4.  Camurati-Engelmann Disease.

Authors:  Wim Van Hul; Eveline Boudin; Filip M Vanhoenacker; Geert Mortier
Journal:  Calcif Tissue Int       Date:  2019-02-05       Impact factor: 4.333

5.  Camurati-Engelmann disease: imaging, clinical features and differential diagnosis.

Authors:  Aldona Bartuseviciene; Arturas Samuilis; Jovitas Skucas
Journal:  Skeletal Radiol       Date:  2009-02-12       Impact factor: 2.199

6.  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

7.  Camurati-Engelmann disease-a rare cause of tetany identified on bone scintigraphy: A case report.

Authors:  Peng Xie; Jian-Min Huang; Huan-Li Li; Xiao-Jie Huang; Ling-Ge Wei
Journal:  Medicine (Baltimore)       Date:  2017-07       Impact factor: 1.889

8.  Orthopedic Manifestations of Type I Camurati-Engelmann Disease.

Authors:  Alisher J Yuldashev; Chang Ho Shin; Yong Sung Kim; Woo Young Jang; Moon Seok Park; Jong Hee Chae; Won Joon Yoo; In Ho Choi; Ok Hwa Kim; Tae-Joon Cho
Journal:  Clin Orthop Surg       Date:  2017-02-13

9.  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

10.  A patient with Camurati-Engelmann disease presenting bilateral TMJ ankylosis: A case report.

Authors:  Nour J Salman; Denis Pimenta E Souza; Erika Kuriki; Eduardo Sant'Ana
Journal:  Int J Surg Case Rep       Date:  2020-08-19
  10 in total

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