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Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder)
Spondyloepimetaphyseal dysplasia with multiple dislocations
Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type
Spondyloepimetaphyseal dysplasia with joint laxity type 2
Spondyloepimetaphyseal dysplasia with joint laxity Hall type
Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type
A rare genetic primary bone dysplasia disorder characterized by midface hypoplasia, short stature, generalized joint laxity, multiple joint dislocations (most frequently of knees and hips), limb malalignment (genu valgum/varum) and progressive spinal deformity (for example kyphosis/scoliosis). Radiography reveals distinctive slender metacarpals and metatarsals, as well as small, irregular epiphyses, metaphyseal irregularities with vertical striations, constricted femoral necks and mild platyspondyly among others.
spondylo-epimetafysaire dysplasie met meervoudige luxaties
spondylo-epimetafysaire dysplasie met gewrichtslaxiteit type 2
spondylo-epimetafysaire dysplasie met gewrichtslaxiteit type Hall
SEMD met meervoudige luxaties
Id766820007
StatusPrimitive
Associated morphologyDysplasia
Finding siteBone structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDislocation
Finding siteJoint structure of multiple body sites
Clinical courseProgressive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ77.7
RuleTRUE
AdviceALWAYS Q77.7
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ68.8
RuleTRUE
AdviceALWAYS Q68.8
CorrelationSNOMED CT source code to target map code correlation not specified