Toriello-Carey syndrome (Q94219): Difference between revisions
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Síndrome de Toriello Carey é caracterizada por agenesia do corpo caloso, telecanto, fissuras palpebrais curtas, nariz pequeno com narinas antevertidas, sequência de Pierre Robin (incluindo fenda palatina), orelhas de formato anormal, pele do pescoço redundante, anomalias laríngeas, defeitos cardíacos, mãos curtas, e hipotonia. | |||
| description / en | description / en | ||
Toriello Carey syndrome is characterised by agenesis of corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, Pierre Robin sequence (including a cleft palate), abnormally shaped ears, redundant neck skin, laryngeal anomalies, cardiac defects, short hands, and hypotonia. | |||
Revision as of 09:21, 16 August 2026
Toriello Carey syndrome is characterised by agenesis of corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, Pierre Robin sequence (including a cleft palate), abnormally shaped ears, redundant neck skin, laryngeal anomalies, cardiac defects, short hands, and hypotonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_147297969 |
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| English | Toriello-Carey syndrome |
Toriello Carey syndrome is characterised by agenesis of corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, Pierre Robin sequence (including a cleft palate), abnormally shaped ears, redundant neck skin, laryngeal anomalies, cardiac defects, short hands, and hypotonia. |
