Mesomelic dysplasia, Langer type (Q101940): Difference between revisions
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A displasia mesomélica de Langer (LMD) é caracterizada por baixa estatura desproporcional grave com encurtamento mesomélico e rizomélico dos membros superiores e inferiores. LMD representa uma forma mais grave de discondrosteose de Léri-Weill (ver este termo) com ossos longos dos membros gravemente encurtados (envolvendo os segmentos médio e proximal), deformidade da cabeça do úmero, angulação da diáfise radial, distorção do carpo , colo femoral curto e ausência ou hipoplasia da metade proximal da fíbula. | |||
| description / en | description / en | ||
Langer mesomelic dysplasia (LMD) is characterised by severe disproportionate short stature with mesomelic and rhizomelic shortening of the upper and lower limbs. LMD represents a more severe form of L eri-Weill dyschondrosteosis (see this term) with severely shortened long bones of the limbs (involving both the middle and proximal segments), deformity of the humeral head, angulation of the radial shaft, carpal distortion, a short femoral neck, and absence or hypoplasia of the proximal half of the fibula. | |||
Revision as of 18:47, 16 August 2026
Langer mesomelic dysplasia (LMD) is characterised by severe disproportionate short stature with mesomelic and rhizomelic shortening of the upper and lower limbs. LMD represents a more severe form of L eri-Weill dyschondrosteosis (see this term) with severely shortened long bones of the limbs (involving both the middle and proximal segments), deformity of the humeral head, angulation of the radial shaft, carpal distortion, a short femoral neck, and absence or hypoplasia of the proximal half of the fibula.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_83297413 |
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| English | Mesomelic dysplasia, Langer type |
Langer mesomelic dysplasia (LMD) is characterised by severe disproportionate short stature with mesomelic and rhizomelic shortening of the upper and lower limbs. LMD represents a more severe form of L eri-Weill dyschondrosteosis (see this term) with severely shortened long bones of the limbs (involving both the middle and proximal segments), deformity of the humeral head, angulation of the radial shaft, carpal distortion, a short femoral neck, and absence or hypoplasia of the proximal half of the fibula. |
