Abstract
Meyer's dysplasia strongly mimics Legg-CalvePerthes' disease despite differing markedly in eventual outcome. This study presents the clinicoradiological features which differentiate it from Perthes' disease in a group of 178 children with a preliminary diagnosis of Perthes' disease, of whom nine were subsequently diagnosed with Meyer's dysplasia. All had a near normal development of the femoral head ; mild flattening was seen in two cases. Clinical initial presentation often resembles Perthes' disease. However, the presence of a granular aspect of the femoral head, often bilateral, in a male child with a preliminary diagnosis of Perthes' disease should alert the clinician to the possibility of Meyer's dysplasia. Restitution of normal capital architecture is usual ; there may however be a mild residual hypoplasia.
| Original language | English |
|---|---|
| Pages (from-to) | 608-612 |
| Number of pages | 5 |
| Journal | Acta Orthopaedica Belgica |
| Volume | 76 |
| Issue number | 5 |
| Publication status | Published - 2010 Oct 1 |
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Keywords
- Bilateral
- Delayed ossification
- Granular pattern
- Meyer's dysplasia
- Perthes' disease
ASJC Scopus subject areas
- Orthopedics and Sports Medicine
Cite this
Meyer's dysplasia : Delayed ossification of the femoral head as a differential diagnosis in Perthes' disease. / Muzaffar, Nasir; Song, Hae Ryong; Devmurari, Kamlesh; Modi, Hitesh.
In: Acta Orthopaedica Belgica, Vol. 76, No. 5, 01.10.2010, p. 608-612.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Meyer's dysplasia
T2 - Delayed ossification of the femoral head as a differential diagnosis in Perthes' disease
AU - Muzaffar, Nasir
AU - Song, Hae Ryong
AU - Devmurari, Kamlesh
AU - Modi, Hitesh
PY - 2010/10/1
Y1 - 2010/10/1
N2 - Meyer's dysplasia strongly mimics Legg-CalvePerthes' disease despite differing markedly in eventual outcome. This study presents the clinicoradiological features which differentiate it from Perthes' disease in a group of 178 children with a preliminary diagnosis of Perthes' disease, of whom nine were subsequently diagnosed with Meyer's dysplasia. All had a near normal development of the femoral head ; mild flattening was seen in two cases. Clinical initial presentation often resembles Perthes' disease. However, the presence of a granular aspect of the femoral head, often bilateral, in a male child with a preliminary diagnosis of Perthes' disease should alert the clinician to the possibility of Meyer's dysplasia. Restitution of normal capital architecture is usual ; there may however be a mild residual hypoplasia.
AB - Meyer's dysplasia strongly mimics Legg-CalvePerthes' disease despite differing markedly in eventual outcome. This study presents the clinicoradiological features which differentiate it from Perthes' disease in a group of 178 children with a preliminary diagnosis of Perthes' disease, of whom nine were subsequently diagnosed with Meyer's dysplasia. All had a near normal development of the femoral head ; mild flattening was seen in two cases. Clinical initial presentation often resembles Perthes' disease. However, the presence of a granular aspect of the femoral head, often bilateral, in a male child with a preliminary diagnosis of Perthes' disease should alert the clinician to the possibility of Meyer's dysplasia. Restitution of normal capital architecture is usual ; there may however be a mild residual hypoplasia.
KW - Bilateral
KW - Delayed ossification
KW - Granular pattern
KW - Meyer's dysplasia
KW - Perthes' disease
UR - http://www.scopus.com/inward/record.url?scp=78549273995&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78549273995&partnerID=8YFLogxK
M3 - Article
C2 - 21138215
AN - SCOPUS:78549273995
VL - 76
SP - 608
EP - 612
JO - Acta Orthopaedica Belgica
JF - Acta Orthopaedica Belgica
SN - 0001-6462
IS - 5
ER -