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         Encephalofacial Angiomatosis:     more detail

81. Malattie Rare E Genetiche Lettera "W"
angioma/ectoneurodermal hamartoma/encephalocraniofacial angiomatosis/encephalofacialangiomatosis/encephalofacial neuroangiomatosis/encephalotrigeminal
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82. DermIS / Hauptmenü / DOIA / Sturge-Weber-Krabbe-Syndrom / Info
Translate this page oculo - orbital - thalamo - encephalic syndrome, angiomatosis, encephalocutaneous,angiomatosis, encephalofacial, angiomatosis, encephalotrigeminal, DIMITRI
http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=d&diagnr=759610&topic

83. HONselect - Sturge-Weber Syndrome
Translate this page angiomatosis Oculoorbital-Thalamic Syndrome - encephalofacial HemangiomatosisSyndrome - Meningo-Oculo-Facial angiomatosis
http://www.hon.ch/HONselect/RareDiseases/C04.557.645.375.850.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Sturge-Weber Syndrome - Neuroretinoangiomatosis
- Phakomatosis, Sturge-Weber
- Angiomatosis Oculoorbital-Thalamic Syndrome
- Encephalofacial Hemangiomatosis Syndrome
- Meningo-Oculo-Facial Angiomatosis
- Meningofacial Angiomatosis-Cerebral Calcification Syndrome
Français: Syndrome de Sturge-Weber-Krabbe - Syndrome de Sturge-Weber - Angiomatose congénitale de Sturge-Weber-Krabbe - Angiomatose méningo-rétino-faciale - Angiomatose neurocutanée de Sturge-Weber-Krabbe - Maladie de Sturge-Weber-Krabbe - Phacomatose de Sturge-Weber-Krabbe Deutsch: Sturge-Weber-Syndrom - Hamartome, ektoneurodermale - Neuroektodermaldysplasie, kongenitale - Neurokutanes Syndrom - Neuroretinoangiomatose - Phakomatose, Sturge-Weber - Angiomatosis encephalofacialis Español: Síndrome de Sturge-Weber - Facomatosis de Sturge-Weber - Neurorretinoangiomatosis Português: Síndrome de Sturge-Weber - Facomatose de Sturge-Weber - Neurorretinoangiomatose HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C04.557.645.375.850.html

84. Sturge-Weber Syndrome
encephalofacial hemangiomatosis syndrome. Meningofacial angiomatosis cerebralcalcification syndrome. Neuroretinoangiomatosis. Sturge disease
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=284

85. Sturge-Weber Syndrome Topic - Unified Search Environment
angiomatosis, encephalofacial DXP/SY/NOCODE DIMITRI DISEASE DXP/SY/NOCODEPhakomatosis, SturgeWeber MSH/EP/D013341 DXP/SY/NOCODE MSH/PM/D013341
http://www.use.hcn.com.au/portals/shared/subject.`Sturge-Weber Syndrome`/home.ht
Sturge-Weber Syndrome Topic Tree Definition:
A congenital syndrome characterized by a port-wine nevus covering portions of the face and cranium (in the distribution of the ophthalmic division of the TRIGEMINAL NERVE) and angiomas of the meninges and choroid. Clinical manifestations include the onset of focal SEIZURES, progressive hemiparesis, GLAUCOMA, hemianopsia, and cognitive deficits in the first decade of life. By age two years, skull radiographs reveal "tramline calcifications" of the margins of the occipital and parietal lobes. Pathologically cortical neurons are replaced by glial tissue that undergoes calcification. (From Adams et al., Principles of Neurology, 6th ed, pp1018-9) Synonyms and Source Vocabularies:
Sturge-Weber Syndrome
ANGIOMATOSIS, ENCEPHALOTRIGEMINAL
Sturge's Syndrome
Sturge-Kalischer-Weber Syndrome
STURGE-WEBER DISEASE
Sturge Disease
Sturge-Weber-Dimitri Syndrome
ANGIOMATOSIS, ENCEPHALOFACIAL
DIMITRI DISEASE Phakomatosis, Sturge-Weber Neuroretinoangiomatosis Meningofacial Angiomatosis-Cerebral Calcification Syndrome Meningo-Oculo-Facial Angiomatosis Angiomatosis Oculoorbital-Thalamic Syndrome Encephalofacial Hemangiomatosis Syndrome Sturge-Weber-Krabbe Syndrome neurocutaneous syndrome Parkes Weber syndrome Weber syndrome Vascular Diseases

86. Entrez PubMed
The case of a 21year-old woman who was affected by both encephalofacialangiomatosis (Sturge-Weber
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3

87. Log In Problems
SturgeWeber syndrome, also known as encephalofacial/encephalotrigeminalangiomatosis, is characterized by a facial port wine nevus and leptomeningeal
http://www.medscape.com/viewarticle/438132_print
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88. Sturge-Weber Syndrome - Neuroretinoangiomatosis - Information Page With HONselec
Synonym(s) Neuroretinoangiomatosis / Phakomatosis, SturgeWeber / AngiomatosisOculoorbital-Thalamic Syndrome / encephalofacial Hemangiomatosis Syndrome
http://www.hon.ch/HONselect/RareDiseases/EN/C04.557.645.375.850.html
InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese
the word the part of word in MeSH term in MeSH term and description Information on "Sturge-Weber Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese
Sturge-Weber Syndrome Definition: A congenital syndrome characterized by a port-wine nevus covering portions of the face and cranium (in the distribution of the ophthalmic division of the TRIGEMINAL NERVE ) and angiomas of the meninges and choroid. Clinical manifestations include the onset of focal SEIZURES , progressive hemiparesis, GLAUCOMA , hemianopsia, and cognitive deficits in the first decade of life. By age two years, skull radiographs reveal "tramline calcifications" of the margins of the occipital and parietal lobes. Pathologically cortical neurons are replaced by glial tissue that undergoes calcification. (From Adams et al., Principles of Neurology, 6th ed, pp1018-9)
Synonym(s): Neuroretinoangiomatosis / Phakomatosis, Sturge-Weber / Angiomatosis Oculoorbital-Thalamic Syndrome / Encephalofacial Hemangiomatosis Syndrome /

89. Portal Toolkit Invalid Site URL
Novotny EJ, Urich H. The coincidence of neurocutaneous melanosis and encephalofacialangiomatosis. Clin. Neuropathol. 1986; 5 24651.
http://ppv.ovid.com/pt/re/aujd/fulltext.00000936-200105000-00011.htm
Sorry, the URL specified, http://ppv.ovid.com:80/pt/re/aujd/fulltext.00000936-200105000-00011.htm , is invalid.

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90. [ ¥x¥_ºaÁ`¡E¤p¨à¯«¸g¥~¬ì ] = [ Pediatric Neurosurgery Of VGH Taipe
The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set.
http://www.vghtpe.gov.tw/~pns/learn/01/01_027.htm
¸£»PC­±ªº¦åºÞ½F¯f ¸£»PC­±ªº¦åºÞ½F¯f¡]Encephalofacial angiomatosis, Encephalotrigeminal angiomatosis, Sturge-Weber syndrome, SWS¡^»P¨ä¥L¥À¯Z¯g¤£¦P¡AÄÝ«D¿ò¶Ç©Ê¯e¯f¡Aµo¥Íªº­ì¦]¤£©ú¡C
¯S¼x¬OÁy¤Wªº¬õ°s¦âµi¡]port wine stain, port wine nevus, nevus flammeus¡APWS¡^¡A¦P°¼¤j¸£³n¸£½¤¦åºÞ½F¡]pia angioma¡^¡A¸£²Õ´¤Î¥Ö½è¶t¤Æ¡]cortical calcification¡^¡A±`¦³§½³¡©ÊÅöíwµo§@¡]partial seizure¡^©Î¦¸µo©ÊªxµoÅöíwµo§@¡]seconadary generalized siezure¡^¡Aº¥¶iªº¹ï°¼°¾Åõ¡]hemiparesis¡^¡A¥bª¼¡]hemianopsia¡^¡A«C¥ú²´¡]glaucoma¡^¡A¯ßµ¸½¤¦åºÞ½F¡]choroidal angiomatosis¡^¡A¤Î´¼¯à»Ùª¡C Áy¤W¤§¬õ°s¦âµi³q±`µo¥Í©ó³æ°¼Áy¤W³¡¡B¤W²´¥Ö¡B©Î²´²µ¤W¤è¡C¬õ°s¦âµi¡]PWS¡^¡A¥iµo¥Í©ó¨­Åé¨ä¥L³B¥Ö½§¡A¦ýµ´¤j³¡¤Àµo¥Í©ó¤T¤e¯«¸g¥Ö°Ï¡]trigeminal dermatome¡^¡A¨ä¤¤¯­¦³8%¦³²´²y©Î¤¤¼Ï¯«¸g¨t²Î¯gª¬¡CÆ`°©X¥ú¥i¯à¬Ý¨ì¸£¥Ö½è¶t¤Æªº¹q¨®­y¸ñ¼Ò¼Ë¡]tram track pattern¡^¡C ¥»¯¸©Ò¦³¹Ï¡B¤å¸ê®Æ§¡ÄÝ­ì§@ªÌ©Ò¦³¡A½Ð¤Å¾Õ¦Û«þ¨©

91. Neurocutaneous Melanosis Presenting With Intracranial Amelanotic Melanoma -- Van
Novotny EJ, Urich H. The coincidence of neurocutaneous melanosis and encephalofacialangiomatosis. Clin Neuropathol 1986;5246251Medline
http://www.ajnr.org/cgi/content/full/20/3/457
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ARTICLE
Neurocutaneous Melanosis Presenting with Intracranial Amelanotic Melanoma
Bart D. Vanzieleghem ,a Marc M. Lemmerling a and Rudy N. Van Coster a a From the Departments of Radiology (B.D.V., M.M.L.) and Pediatrics (R.N.V.C.), University Hospital Gent, Belgium.
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Abstract
Case Report
Discussion
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Summary: We describe imaging findings in a 2-year-old girl with neurocutaneous melanosis and malignant cerebral melanoma. Because the cerebral melanoma in this child was of the amelanotic type, high-signal intensity on unenhanced T1-weighted images was not present. The cutaneous lesions played a crucial role in establishing

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