| Descriptor English: | Sturge-Weber Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Sturge-Weber
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| Descriptor Portuguese: | Síndrome de Sturge-Weber | ||||||
| Descriptor French: | Syndrome de Sturge-Weber | ||||||
| Entry term(s): |
Angiomatosis Oculoorbital-Thalamic Syndrome Angiomatosis, Meningo-Oculo-Facial Encephalofacial Hemangiomatosis Syndrome Hemangiomatosis Syndrome, Encephalofacial Meningo Oculo Facial Angiomatosis Meningo-Oculo-Facial Angiomatosis Meningofacial Angiomatosis-Cerebral Calcification Syndrome Neuroretinoangiomatosis Parkes Weber Syndrome Parkes-Weber Syndrome Phakomatosis, Sturge Weber Phakomatosis, Sturge-Weber Sturge Disease Sturge Kalischer Weber Syndrome Sturge Syndrome Sturge Weber Dimitri Syndrome Sturge Weber Krabbe Syndrome Sturge Weber Syndrome Sturge's Syndrome Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis Sturge-Weber-Dimitri Syndrome Sturge-Weber-Krabbe Syndrome Syndrome, Encephalofacial Hemangiomatosis Syndrome, Parkes Weber Syndrome, Parkes-Weber Syndrome, Sturge Syndrome, Sturge's Syndrome, Sturge-Kalischer-Weber Syndrome, Sturge-Weber Syndrome, Sturge-Weber-Dimitri Syndrome, Sturge-Weber-Krabbe |
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| Tree number(s): |
C04.557.645.375.850 C10.562.800 C14.907.077.850 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D013341 | ||||||
| Scope note: | A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 91; was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93 |
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| Online Note: | search ANGIOMATOSIS 1966-74; use STURGE-WEBER SYNDROME to search DIMITRI DISEASE 1989-93 |
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| History Note: | 91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93 |
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| DeCS ID: | 24333 | ||||||
| Unique ID: | D013341 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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DISEASES
Neoplasms [C04]Neoplasms
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Sturge-Weber Syndrome
- Preferred
| Concept UI |
M0020641 |
| Scope note | A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. |
| Preferred term | Sturge-Weber Syndrome |
| Entry term(s) |
Angiomatosis Oculoorbital-Thalamic Syndrome Angiomatosis, Meningo-Oculo-Facial Encephalofacial Hemangiomatosis Syndrome Hemangiomatosis Syndrome, Encephalofacial Meningo Oculo Facial Angiomatosis Meningo-Oculo-Facial Angiomatosis Meningofacial Angiomatosis-Cerebral Calcification Syndrome Neuroretinoangiomatosis Parkes Weber Syndrome Parkes-Weber Syndrome Phakomatosis, Sturge Weber Phakomatosis, Sturge-Weber Sturge Disease Sturge Kalischer Weber Syndrome Sturge Syndrome Sturge Weber Dimitri Syndrome Sturge Weber Krabbe Syndrome Sturge Weber Syndrome Sturge's Syndrome Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis Sturge-Weber-Dimitri Syndrome Sturge-Weber-Krabbe Syndrome Syndrome, Encephalofacial Hemangiomatosis Syndrome, Parkes Weber Syndrome, Parkes-Weber Syndrome, Sturge Syndrome, Sturge's Syndrome, Sturge-Kalischer-Weber Syndrome, Sturge-Weber Syndrome, Sturge-Weber-Dimitri Syndrome, Sturge-Weber-Krabbe |
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