- A case of acro-osteolysis caused by peripheral neuropathy after minor burn injury
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Yang MJ, Seo JH, Lee JS, Kim TS, Lee JW, Jung JW, Kim GT
- KMID: 2258156
- Korean J Med.
- 2009 Aug;77(Suppl 1):S245-S248.
Acro-osteolysis is characterized by bone resorption in the fingers and toes and can occur in several diseases. Occupational exposure to polyvinyl chloride polymers, thermal injury, and repetitive mechanical injury can... -
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- Effect of Zoledronic Acid on Acro-Osteolysis and Osteoporosis in a Patient with Hajdu-Cheney Syndrome
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Hwang S, Shin DY, Moon SH, Lee EJ, Lim SK, Kim OH, Rhee Y
- KMID: 1777031
- Yonsei Med J.
- 2011 May;52(3):543-546.
- doi: 10.3349/ymj.2011.52.3.543
Hajdu-Cheney syndrome is a rare, autosomal dominant skeletal dysplasia marked by acro-osteolysis of the distal phalanges and severe osteoporosis. Although there are more than 60 reports published to date, proper... -
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- Acrogeria
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Chun SC, Kang WH, Kim HJ
- KMID: 2230588
- Korean J Dermatol.
- 1998 Apr;36(2):350-354.
We report a case of a 41-year-old female with acrogeria. She was in good health except for the prominent atrophy over the hands and feet. On microscopic examination of a... -
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- Pyknodysostosis: report of a rare case with review of literature
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Ramaiah KK, George GB, Padiyath S, Sethuraman R, Cherian B
- KMID: 2167404
- Imaging Sci Dent.
- 2011 Dec;41(4):177-181.
- doi: 10.5624/isd.2011.41.4.177
Pyknodysostosis is a rare autosomal recessive disorder characterized by the post natal onset of short limbs, short stature, and generalized hyperostosis along with acro-osteolysis with sclerosis of the terminal phalanges,... -
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- Bone and Joint changes following Electrical Burn: Plain Radiographic findings
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Kim UJ, Lee ES, Shim YS, Kim SB, Lee SH, Jung HK, Hwang DH, Kang IW
- KMID: 2201234
- J Korean Radiol Soc.
- 1998 Oct;39(4):801-805.
- doi: 10.3348/jkrs.1998.39.4.801
PURPOSE: To evaluate the plain radiographic findings of bone and joint changes following electrical burn. MATERIALS AND METHODS: This study involved 19 patients with 27 bone and joints regions which... -
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- Pycnodysostosis with Multi-Segmental Spinal Canal Stenosis due to Ossification of the Yellow Ligament
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Wada K, Kanaya K, Murata Y, Kato Y
- KMID: 2270174
- Asian Spine J.
- 2015 Apr;9(2):286-289.
- doi: 10.4184/asj.2015.9.2.286
Pycnodysostosis is an autosomal recessive disorder characterized by osteosclerosis, small stature, acro-osteolysis of the distal phalanges, loss of the mandibular angle, separated cranial sutures with open fontanels, and frequent fractures.... -
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- A Case of Acroosteolysis in Primary Hypertrophic Osteoarthropathy
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Lee HJ, Kim HJ, Hwang CG, Choi JH, Kang EJ
- KMID: 2297540
- J Rheum Dis.
- 2013 Aug;20(4):247-250.
- doi: 10.4078/jrd.2013.20.4.247
Primary hypertrophic osteoarthropathy or pachydermoperiostosis is a rare hereditary disorder characterized by digital clubbing, pachydermia and periostosis. Its precise incidence and prevalence is still unknown due to the lack of... -
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- A Case of Hereditary Sensory Neuropathy Type II with Acroosteolysis
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Seo JH, Song CH, Park CS, Lee CH, Lee JS, Kim TS, Lee SK
- KMID: 1542342
- J Korean Rheum Assoc.
- 1997 Jan;4(1):105-110.
The hereditary sensory neuropathy is a very rare disease characterized by prominent sensory loss without corresponding motor involvement, but may be associated with autonomic features. Currently, the disease is divided... -
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- Successful Treatment of Newly Developed, Intractable Digital Ulcers and Gangrene with Bosentan in Systemic Sclerosis
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Tag HS, Jun SM, Lee SG, Park EK, Koo DW, Kim GT
- KMID: 2326736
- J Rheum Dis.
- 2016 Jun;23(3):193-197.
- doi: 10.4078/jrd.2016.23.3.193
In systemic sclerosis, digital ulcers and gangrene are somewhat common clinical characteristics of obliterative vasculopathy. These manifestations increase morbidities, such as pain, infections, and acroosteolysis. However, patient responses to the... -
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- Acroosteolysis of Scleroderma Associated with a Felon
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Hwang IH, Lim MS, Kim KY, Kim HC, Moon SH, Lee JH, Cho SJ
- KMID: 2185600
- J Korean Orthop Assoc.
- 2010 Feb;45(1):88-91.
- doi: 10.4055/jkoa.2010.45.1.88
The Scleroderma is a chronic inflammatory disease of the connective tissue with involvement of the skin and other organs. It can be a manifestation of various disorders and occasionally acroosteolysis... -
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- Pachydermoperiostosis in a 19 Year-old Boy Presenting as an Acromegaly-like Syndrome
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Lim JS, Lee JA, Kim DH, Lim KJ, Jeun DG
- KMID: 1568761
- J Korean Soc Pediatr Endocrinol.
- 2004 Dec;9(2):213-219.
A nineteen year-old boy with progressive enlargement of the joints and distal extremities, clubbing, coarse facial features and hyperhidrosis was investigated. In physical examination, thickening of the scalp with furrowing... -
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- A Case of Sjogren Syndrome Associated with Acroosteolysis
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Hong YS, Yang HI, Park SH, Lee SH, Cho CS, Kim HY
- KMID: 2025516
- J Korean Rheum Assoc.
- 1996 Jan;3(1):92-96.
Acroosteolysis (AOL) refers to a destructive process involving distal phalangeal shaft while the tuft and base are preserved. It can be a manifestation of various diseases, such as scleroderma, Raynaud's... -
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- A Case Report of Hajdu-Cheney Syndrome
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Han EJ, Mun JI, An SY, Jung YJ, Kim OH, Chung YS
- KMID: 2169023
- Endocrinol Metab.
- 2010 Jun;25(2):152-156.
- doi: 10.3803/EnM.2010.25.2.152
Hajdu-Cheney syndrome (HCS) is a rare skeletal dysplasia that is characterized by acroosteolysis of the distal phalanges, distinctive craniofacial and skull changes, dental abnormalities and generalized osteoporosis. The clinical and... -
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