Add to ORKGThe authors describe the case of an Italian male aged 19 years who came to their observation for severe limping with reduction in hip movement and spondyloepiphyseal radiographic modifications of an osteochondrodysplastic origin. The studies carried out led to a diagnosis of spondyloepiphyseal dysplasia tarda (SEDT)
Background: Skeletal dysplasia's cause significant neurological symptoms and disrupt the development...
Sedaghatian type spondylometaphyseal dysplasia is a rare osteochondrodysplasia first described in 19...
Objective. Spondyloepiphyseal dysplasia tarda (SEDT) is a rare hereditary bone disease characterized...
The authors describe the case of an Italian male aged 19 years who came to their observation for sev...
Spondyloepiphyseal dysplasia tarda (SEDT), which is characterized by short stature with short trunk,...
Spondyloepiphysial dysplasia (SED) is a rare diseases which causes delayed growth, short statue and ...
Spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) is a rare autosomal recess...
Giriş: Spondiloepifizyal displazi (SED) sıklıkla erken başlangıçlı osteoartrozis ile ilişkili geneti...
The X-linked form of spondyloepiphyseal dysplasia tarda (SEDL), a radiologically distinct skeletal d...
The X-linked form of spondyloepiphyseal dysplasia tarda (SEDL), a radiologically distinct skeletal d...
Spondyloepiphyseal dysplasia tarda (SEDL) is an X-linked recessive osteochondropdysplasia. It is a p...
Spondyloepiphyseal dysplasia tarda (SEDL) is a radiologically distinct, X-chromosome linked primary ...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
PubMed ID: 10870664Spondyloepiphyseal dysplasia tarda with progressive arthropathy, described by Wyn...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Background: Skeletal dysplasia's cause significant neurological symptoms and disrupt the development...
Sedaghatian type spondylometaphyseal dysplasia is a rare osteochondrodysplasia first described in 19...
Objective. Spondyloepiphyseal dysplasia tarda (SEDT) is a rare hereditary bone disease characterized...
The authors describe the case of an Italian male aged 19 years who came to their observation for sev...
Spondyloepiphyseal dysplasia tarda (SEDT), which is characterized by short stature with short trunk,...
Spondyloepiphysial dysplasia (SED) is a rare diseases which causes delayed growth, short statue and ...
Spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) is a rare autosomal recess...
Giriş: Spondiloepifizyal displazi (SED) sıklıkla erken başlangıçlı osteoartrozis ile ilişkili geneti...
The X-linked form of spondyloepiphyseal dysplasia tarda (SEDL), a radiologically distinct skeletal d...
The X-linked form of spondyloepiphyseal dysplasia tarda (SEDL), a radiologically distinct skeletal d...
Spondyloepiphyseal dysplasia tarda (SEDL) is an X-linked recessive osteochondropdysplasia. It is a p...
Spondyloepiphyseal dysplasia tarda (SEDL) is a radiologically distinct, X-chromosome linked primary ...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
PubMed ID: 10870664Spondyloepiphyseal dysplasia tarda with progressive arthropathy, described by Wyn...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Background: Skeletal dysplasia's cause significant neurological symptoms and disrupt the development...
Sedaghatian type spondylometaphyseal dysplasia is a rare osteochondrodysplasia first described in 19...
Objective. Spondyloepiphyseal dysplasia tarda (SEDT) is a rare hereditary bone disease characterized...