Spondylometaphyseal dysplasia, Schmidt type (Q52460): Difference between revisions
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Displasia espondilometafisária, tipo Schmidt é uma displasia esquelética caracterizada por baixa estatura, geno valgo grave, pelve pequena, cifoescoliose progressiva, deformidade de punho, miopia, ossos longos curtos e displasia metafisária grave com alterações espinais moderadas e alterações mínimas em mãos e pés. | |||
| description / en | description / en | ||
Spondylometaphyseal dysplasia, Schmidt type is a skeletal dysplasia characterised by short stature, severe genu valgum, small pelvis, progressive kypho-scoliosis, wrist deformity, myopia, short long bones, and severe metaphyseal dysplasia with moderate spinal changes and minimal changes in the hands and feet. | |||
Revision as of 23:44, 13 August 2026
Spondylometaphyseal dysplasia, Schmidt type is a skeletal dysplasia characterised by short stature, severe genu valgum, small pelvis, progressive kypho-scoliosis, wrist deformity, myopia, short long bones, and severe metaphyseal dysplasia with moderate spinal changes and minimal changes in the hands and feet.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1092012084 |
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| English | Spondylometaphyseal dysplasia, Schmidt type |
Spondylometaphyseal dysplasia, Schmidt type is a skeletal dysplasia characterised by short stature, severe genu valgum, small pelvis, progressive kypho-scoliosis, wrist deformity, myopia, short long bones, and severe metaphyseal dysplasia with moderate spinal changes and minimal changes in the hands and feet. |
