Roberts syndrome (Q94209): Difference between revisions
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Síndrome de Roberts é uma síndrome de anomalias do desenvolvimento caracterizada por retardo de crescimento pré e pós-natal, graves defeitos simétricos de redução dos membros, anomalias craniofaciais e déficit intelectual grave. A focomelia SC é uma forma mais branda de RBS. | |||
| description / en | description / en | ||
Roberts syndrome is a developmental anomalies syndrome characterised by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS. | |||
Revision as of 09:20, 16 August 2026
Roberts syndrome is a developmental anomalies syndrome characterised by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2130958672 |
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| English | Roberts syndrome |
Roberts syndrome is a developmental anomalies syndrome characterised by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS. |
