Thoracolumbosacral spina bifida cystica with hydrocephalus (Q64718): Difference between revisions
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| description / pt-br | description / pt-br | ||
Condição causada pela falha do tubo neural em se desenvolver corretamente durante o período pré-natal. Esta condição é caracterizada por danos neurais e hidrocefalia. Essa condição também pode se manifestar com siringomielia, luxação do quadril, dor de cabeça, náuseas, vômitos, visão embaçada, problemas de equilíbrio, problemas de controle da bexiga ou deficiência mental. Esta doença pode estar associada a mutações no gene FUZ. | |||
| description / en | description / en | ||
A condition caused by failure of the neural tube to correctly develop during the antenatal period. This condition is characterised by nerve damage and hydrocephalus. This condition may also present with syringomyelia, hip dislocation, headache, nausea, vomiting, blurry vision, balance problems, bladder control problems, or mental impairment. This disease may be associated with mutations in the FUZ gene. | |||
Revision as of 12:25, 14 August 2026
A condition caused by failure of the neural tube to correctly develop during the antenatal period. This condition is characterised by nerve damage and hydrocephalus. This condition may also present with syringomyelia, hip dislocation, headache, nausea, vomiting, blurry vision, balance problems, bladder control problems, or mental impairment. This disease may be associated with mutations in the FUZ gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_239087239 |
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| English | Thoracolumbosacral spina bifida cystica with hydrocephalus |
A condition caused by failure of the neural tube to correctly develop during the antenatal period. This condition is characterised by nerve damage and hydrocephalus. This condition may also present with syringomyelia, hip dislocation, headache, nausea, vomiting, blurry vision, balance problems, bladder control problems, or mental impairment. This disease may be associated with mutations in the FUZ gene. |
