Carey-Fineman-Ziter syndrome (Q94118): Difference between revisions
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A síndrome de Carey-Fineman-Ziter é uma condição rara caracterizada pela associação de hipotonia, sequência de Moebius (paralisia facial congênita bilateral com comprometimento da abdução ocular), sequência de Pierre-Robin (micrognatia, glossoptose e palato ogival ou fenda palatina), face incomum e retardo de crescimento. | |||
| description / en | description / en | ||
Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay. | |||
Revision as of 09:14, 16 August 2026
Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1784462638 |
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| English | Carey-Fineman-Ziter syndrome |
Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay. |
