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

作者信息

Mondal R K, Karmakar B, Chandra P K, Mukherjee K

机构信息

Department of Pediatrics Medicine, IPGMER and SSKM, Hospital, Kolkata, India.

出版信息

Indian J Pediatr. 2007 Mar;74(3):291-3. doi: 10.1007/s12098-007-0047-5.

DOI:10.1007/s12098-007-0047-5
PMID:17401271
Abstract

Ghosal type hemato-diaphyseal dysplasia is a recently described clinical entity. The authors describe such a case with severe anemia requiring transfusions and with clinical and radiological evidence of diaphyseal dysplasia. Very few such cases are reported in world literature.

摘要

相似文献

1
Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.
Indian J Pediatr. 2007 Mar;74(3):291-3. doi: 10.1007/s12098-007-0047-5.
2
Early manifestation of Ghosal-type hemato-diaphyseal dysplasia.
Pediatr Hematol Oncol. 2003 Jul-Aug;20(5):409-15.
3
Engelmann's disease with optic atrophy.
Indian J Pediatr. 2002 Sep;69(9):823-4. doi: 10.1007/BF02723700.
4
[Transitory myelofibrosis in a case of diaphyseal dysplasia (Camurati-Engelmann's disease) (author's transl)].
Rofo. 1978 Jan;128(1):70-4. doi: 10.1055/s-0029-1230792.
5
Ghosal haemato-diaphyseal dysplasia: a new disorder.
Eur J Pediatr. 1993 Mar;152(3):218-21. doi: 10.1007/BF01956148.
6
[Otolaryngological aspects of Camurati-Engelmann disease (progressive diaphyseal dysplasia): review of literature and report of one case].
Acta Otorrinolaringol Esp. 1994 May-Jun;45(3):207-13.
7
[Ghosal haematodiaphyseal dysplasia: a new case].
Arch Pediatr. 2005 Aug;12(8):1244-8. doi: 10.1016/j.arcped.2005.01.026.
8
Ghosal hematodiaphyseal dysplasia: a rare cause of a myelophthisic anemia.高索儿干骺端发育不良:髓质破坏贫血的一个罕见病因。
Pediatr Blood Cancer. 2010 Dec 1;55(6):1187-90. doi: 10.1002/pbc.22662.
9
Engelmann's disease of bone--a systemic disorder?
Ann Rheum Dis. 1982 Apr;41(2):183-8. doi: 10.1136/ard.41.2.183.
10
Clinical and biochemical studies in Engelmann's disease (progressive diaphyseal dysplasia).
Q J Med. 1977 Apr;46(182):273-94.

引用本文的文献

1
Ghosal Syndrome--Ten Years Follow-up.
Indian J Pediatr. 2015 Jun;82(6):568-9. doi: 10.1007/s12098-014-1654-6. Epub 2015 Jan 20.
2
Ghosal hematodiaphyseal dysplasia-a concise review including an illustrative patient.戈萨尔骨干部造血发育异常——包括一个病例说明的简要综述。
Skeletal Radiol. 2015 Mar;44(3):447-50. doi: 10.1007/s00256-014-1989-0. Epub 2014 Aug 30.
3
Ghosal hematodiaphyseal dysplasia with myelofibrosis.
Indian J Pediatr. 2013 Dec;80(12):1050-2. doi: 10.1007/s12098-012-0872-z. Epub 2012 Sep 15.

本文引用的文献

1
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A mutation affecting the latency-associated peptide of TGFbeta1 in Camurati-Engelmann disease enhances osteoclast formation in vitro.卡-恩二氏病中影响转化生长因子β1潜伏期相关肽的一种突变可增强体外破骨细胞的形成。
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Ghosal haemato-diaphyseal dysplasia: a new disorder.
Eur J Pediatr. 1993 Mar;152(3):218-21. doi: 10.1007/BF01956148.
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