SCARF syndrome (Q94232): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
A síndrome SCARF é caracterizada pela associação de anormalidades esqueléticas, cútis laxa, craniostenose, genitália ambígua, retardo psicomotor e anormalidades faciais. | |||
| description / en | description / en | ||
SCARF syndrome is characterised by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. | |||
Revision as of 09:21, 16 August 2026
SCARF syndrome is characterised by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1075253748 |
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| English | SCARF syndrome |
SCARF syndrome is characterised by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. |
