Legg-Calve-Perthes disease (LCPD) is the term used to describe uni- or bilateral avascular necrosis (AVN) of the femoral head in children.
Genes related to Legg-calvÉ-perthes Disease
Clinical FeaturesTop most frequent phenotypes and symptoms related to Legg-calvÉ-perthes Disease
- Short stature
- Skeletal muscle atrophy
- Abnormality of the dentition
- Delayed skeletal maturation
- Congenital hip dislocation
- Joint dislocation
And another 6 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Legg-calvÉ-perthes Disease Is also known as legg-perthes disease, osteochondrosis of the capital femoral epiphysis, perthes disease, aseptic necrosis of the capital femoral epiphysis, lcp, osteochondritis of the capital femoral epiphysis.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Sources and references
You can check the following sources for additional information.ORPHANET MESH OMIM Rare Disease Search Engine
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEPHROTIC SYNDROME, TYPE 7; NPHS7 MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA