- Regarding Camurati-Engelmann Disease: In Reply
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Yuldashev , Shin CH, Kim YS, Jang WY, Park MS, Chae JH, Yoo WJ, Choi IH, Kim OH, Cho TJ
- KMID: 2405492
- Clin Orthop Surg.
- 2018 Mar;10(1):118-118.
- doi: 10.4055/cios.2018.10.1.118
No abstract available. -
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- Regarding Camurati-Engelmann Disease: To the Editor
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Viana MM, Nunes SV, Fernandes Gomes DCF, de Andrade MAP, de Aguiar
- KMID: 2405491
- Clin Orthop Surg.
- 2018 Mar;10(1):116-117.
- doi: 10.4055/cios.2018.10.1.116
No abstract available. -
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- Camurati-Engelmann's Disease on (99m)Tc-MDP Bone Scan
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Yoon HJ, Oh SW, Paeng JC, Lee Y, Choi IH, Lee DS
- KMID: 1475271
- Nucl Med Mol Imaging.
- 2009 Dec;43(6):596-599.
A 24 year-old female presented for a (99m)Tc-methylene diphosphonatae (MDP) whole body bone scan due to chronic pain in the bilateral lower extremities that has aggravated since 2002. She was... -
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- The First Korean Case of Camurati-Engelmann Disease (Progressive Diaphyseal Dysplasia) Confirmed by TGFB1 Gene Mutation Analysis
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Park SJ, Yoon CS, Park HW, Choi JR, Chung JS, Lee KA
- KMID: 1779212
- J Korean Med Sci.
- 2009 Aug;24(4):737-740.
- doi: 10.3346/jkms.2009.24.4.737
Camurati-Engelmann disease (CED) is an autosomal dominant progressive diaphyseal dysplasia caused by mutations in the transforming growth factor-beta1 (TGFB1) gene. We report the first Korean family with an affected mother... -
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- Orthopedic Manifestations of Type I Camurati-Engelmann Disease
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Yuldashev , Shin CH, Kim YS, Jang WY, Park MS, Chae JH, Yoo WJ, Choi IH, Kim OH, Cho TJ
- KMID: 2412312
- Clin Orthop Surg.
- 2017 Mar;9(1):109-115.
- doi: 10.4055/cios.2017.9.1.109
BACKGROUND: Camurati-Engelmann disease (CED) is a rare genetic skeletal disorder characterized by limb pain, muscle emaciation and weakness, and cortical thickening of the diaphysis of long bones. It is caused... -
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- Progressive diaphyseal dysplasia (Engelmann's disease): report of a case
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Soh MH, Rhee SJ, Won JJ
- KMID: 2463389
- J Korean Radiol Soc.
- 1981 Dec;17(3):549-554.
- doi: 10.3348/jkrs.1981.17.3.549
Progressive diaphyseal dysplasia is a rare condition and radiographic finding provides conclusive proof. Wehave experienced a sporadic case of progressive diaphyseal dysplasia (Engelmann's disase) of 8 year-old Korean girl, confirmed... -
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