Endosteal sclerosis - cerebellar hypoplasia (Q94148): Difference between revisions
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Síndrome de esclerose endosteal - hipoplasia cerebelar é caracterizada por hipoplasia cerebelar congênita, esclerose endosteal, hipotonia, ataxia, atraso de desenvolvimento leve a moderado, baixa estatura, luxação do quadril e distúrbios de erupção dentária. | |||
| description / en | description / en | ||
Endosteal sclerosis - cerebellar hypoplasia syndrome is characterised by congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances. | |||
Revision as of 09:16, 16 August 2026
Endosteal sclerosis - cerebellar hypoplasia syndrome is characterised by congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1999155016 |
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| English | Endosteal sclerosis - cerebellar hypoplasia |
Endosteal sclerosis - cerebellar hypoplasia syndrome is characterised by congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances. |
