Spondyloepiphyseal dysplasia, Maroteaux type (Q88333): Difference between revisions
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Displasia espondiloepifisária, tipo Maroteaux é um tipo muito raro de displasia espondiloepifisária descrita em menos de 10 pacientes até o momento e caracterizada clinicamente por epífises displásicas, baixa estatura surgindo na primeira infância, pescoço curto, mãos e pés curtos e atarracados, escoliose, geno valgo, pelve anormal, osteoporose e osteoartrite. | |||
| description / en | description / en | ||
Spondyloepiphyseal dysplasia, Maroteaux type is a very rare type of spondyloepiphyseal dysplasia described in fewer than 10 patients to date and characterised clinically by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, scoliosis, genu valgum, abnormal pelvis, osteoporosis and osteoarthritis. | |||
Revision as of 14:31, 15 August 2026
Spondyloepiphyseal dysplasia, Maroteaux type is a very rare type of spondyloepiphyseal dysplasia described in fewer than 10 patients to date and characterised clinically by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, scoliosis, genu valgum, abnormal pelvis, osteoporosis and osteoarthritis.
| Language | Label | Description | Also known as |
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| default for all languages | ID_231279233 |
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| English | Spondyloepiphyseal dysplasia, Maroteaux type |
Spondyloepiphyseal dysplasia, Maroteaux type is a very rare type of spondyloepiphyseal dysplasia described in fewer than 10 patients to date and characterised clinically by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, scoliosis, genu valgum, abnormal pelvis, osteoporosis and osteoarthritis. |
