KEGG   DISEASE: Legg-Calve-Perthes Disease
Entry
H01526                      Disease                                
Name
Legg-Calve-Perthes Disease
  Supergrp
Type II collagenopathies [DS:H00520]
Avascular necrosis of femoral head [DS:H01529]
Description
Legg-Calve-Perthes disease (LCPD) is a particular type of femoral head necrosis occurring in children. It is more common among boys, and bilateral involvement occurs in 8-24% of cases. The disease is usually diagnosed among children under age 14 years, with a peak onset between 5 and 8 years of age. There is delayed skeletal maturation and impaired growth. In addition to congenital abnormalities, LCPD is associated with greater risk of cardiovascular diseases and diseases of the blood. Most cases are sporadic, but familial cases have been described. It has been reported that COL2A1 mutations are associated with this disease.
Category
Musculoskeletal disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 15 Diseases of the musculoskeletal system or connective tissue
  Osteopathies or chondropathies
   FB82  Chondropathies
    H01526  Legg-Calve-Perthes Disease
Pathway
hsa04510  Focal adhesion
hsa04512  ECM-receptor interaction
hsa04151  PI3K-Akt signaling pathway
Gene
COL2A1 [HSA:1280] [KO:K19719]
Other DBs
ICD-11: FB82.1
MeSH: D007873
OMIM: 150600
Reference
  Authors
Bansal T, Jaiswal R
  Title
Legg-Calve-Perthes disease: A must know entity for anaesthesiologists.
  Journal
Indian J Anaesth 60:68-9 (2016)
DOI:10.4103/0019-5049.174807
Reference
  Authors
Young ML, Little DG, Kim HK
  Title
Evidence for using bisphosphonate to treat Legg-Calve-Perthes disease.
  Journal
Clin Orthop Relat Res 470:2462-75 (2012)
DOI:10.1007/s11999-011-2240-0
Reference
  Authors
Miyamoto Y, Matsuda T, Kitoh H, Haga N, Ohashi H, Nishimura G, Ikegawa S
  Title
A recurrent mutation in type II collagen gene causes Legg-Calve-Perthes disease in a Japanese family.
  Journal
Hum Genet 121:625-9 (2007)
DOI:10.1007/s00439-007-0354-y
LinkDB

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