Sturge's disease oor Spaans
Sturge's disease
Vertalings in die woordeboek Engels - Spaans
angiomatosis encefalotrigeminal
síndrome Sturge-Weber
Geskatte vertalings
Vertoon algoritmies gegenereerde vertalings
voorbeelde
Advanced filtering
Voorbeelde moet herlaai word.
MEN-IIa, MEN-IIb, von Recklinghausen disease, tuberous sclerosis, and Sturge–Weber disease
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The following are the most common symptoms of tuberous sclerosis, neurofibromatosis, and Sturge-Weber disease.
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Sturge-Weber disease.
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The following are the most common symptoms of tuberous sclerosis, neurofibromatosis, and Sturge-Weber disease.
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The cause of Sturge-Weber disease is unknown and is considered to be sporadic (occurs by chance).
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Neurofibromatosis (NF): Type I, Type II, and schwannomatosis Sturge-Weber disease
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Other symptoms may include numbness, tingling, or weakness in the fingers and toes. Sturge-Weber disease
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Tuberous sclerosis, NF, and Sturge-Weber disease are congenital (present at birth).
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The cause of Sturge-Weber disease is unknown and is considered to be sporadic (occurs by chance).
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Sturge-Weber disease What causes neurocutaneous syndromes?
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Sturge-Weber disease does not affect the other organs of the body.
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Unlike tuberous sclerosis and NF, Sturge-Weber disease does not affect the other organs of the body.
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Tuberous sclerosis, NF, and Sturge-Weber disease are all conditions that are congenital (present at birth).
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TSNF, and Sturge-Weber disease are all conditions that are congenital (present at birth), caused by genetic mutations.
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Other symptoms that may be experienced include numbness, tingling, or weakness in the fingers and toes. Sturge-Weber disease.
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Sometimes, other family members will have hemangiomas (a benign growth that consists of blood vessels) to a lesser degree than the person with Sturge-Weber disease.
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Hemispherectomy during the first few years of life may benefit children with other uncommon, severe forms of epilepsy (such as Rasmussen syndrome or Sturge-Weber disease).
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Sometimes, other family members will have hemangiomas (a benign growth that consists of blood vessels) to a lesser degree than the person with Sturge-Weber disease.
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Sturge-Weber disease. The classic symptom of this disease is a port wine stain located on the child's face, typically near or around the eye and forehead areas.
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Sturge-Weber disease. The classic symptom of this disease is a port wine stain located on the child's face, typically near or around the eye and forehead areas.
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Since tuberous sclerosis, NF, and Sturge-Weber disease are lifelong conditions that are not correctable, management includes focusing on preventing or minimizing deformities and maximizing the person's capabilities at home and in the community.
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Since tuberous sclerosis, NF, and Sturge-Weber disease are lifelong conditions that are not correctable, management includes focusing on preventing or minimizing deformities and maximizing the child's capabilities at home and in the community.
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In patients with retrobulbar tumor, thyroid eye disease, Sturge-Weber Syndrome or any other type of condition that may cause elevated episcleral venous pressure
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Ranked list of diseases related to "Sturge-Weber Syndrome".
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In eyes with primary angle closure glaucoma, or secondary angle-closure glaucoma, including neovascular glaucomas, in patients with retrobulbar tumour, thyroid eye disease, Sturge-Weber Syndrome or any other type of condition that may cause elevated episcleral venous pressure.
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25 sinne gevind in 14 ms. Hulle kom uit baie bronne en word nie nagegaan nie.