Sturge-Weber syndrome with cerebellar involvement

M. Smith Pearl; W. M.A. Abdalla; D. D.M. Lin; A. M. Comi; E. Boltshauser; P. Gailloud; T. A.G.M. Huisman

doi:10.1016/j.neurad.2008.07.008

Sturge-Weber syndrome with cerebellar involvement

M. Smith Pearl, W. M.A. Abdalla, D. D.M. Lin, A. M. Comi, E. Boltshauser, P. Gailloud, T. A.G.M. Huisman

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

Sturge-Weber syndrome is a rare neurocutaneous disorder that typically presents with angiomas involving the face, ocular choroid and ipsilateral supratentorial leptomeninges. Posterior fossa involvement is extremely rare. We present two patients with simultaneous supra- and infratentorial involvement. Magnetic resonance imaging (MRI) and digital subtracted angiography (DSA) findings are discussed.

Original language	English (US)
Pages (from-to)	57-60
Number of pages	4
Journal	Journal of Neuroradiology
Volume	36
Issue number	1
DOIs	https://doi.org/10.1016/j.neurad.2008.07.008
State	Published - Mar 1 2009

Keywords

Cerebral conventional angiography
Magnetic resonance imaging (MRI)
Sturge-Weber syndrome

ASJC Scopus subject areas

Radiological and Ultrasound Technology
Radiology Nuclear Medicine and imaging
Clinical Neurology

Access to Document

10.1016/j.neurad.2008.07.008

Cite this

@article{37c784a546634739b24bc92588ac4542,

title = "Sturge-Weber syndrome with cerebellar involvement",

abstract = "Sturge-Weber syndrome is a rare neurocutaneous disorder that typically presents with angiomas involving the face, ocular choroid and ipsilateral supratentorial leptomeninges. Posterior fossa involvement is extremely rare. We present two patients with simultaneous supra- and infratentorial involvement. Magnetic resonance imaging (MRI) and digital subtracted angiography (DSA) findings are discussed.",

keywords = "Cerebral conventional angiography, Magnetic resonance imaging (MRI), Sturge-Weber syndrome",

author = "{Smith Pearl}, M. and Abdalla, {W. M.A.} and Lin, {D. D.M.} and Comi, {A. M.} and E. Boltshauser and P. Gailloud and Huisman, {T. A.G.M.}",

year = "2009",

month = mar,

day = "1",

doi = "10.1016/j.neurad.2008.07.008",

language = "English (US)",

volume = "36",

pages = "57--60",

journal = "Journal of Neuroradiology",

issn = "0150-9861",

publisher = "Elsevier Masson",

number = "1",

}

TY - JOUR

T1 - Sturge-Weber syndrome with cerebellar involvement

AU - Smith Pearl, M.

AU - Abdalla, W. M.A.

AU - Lin, D. D.M.

AU - Comi, A. M.

AU - Boltshauser, E.

AU - Gailloud, P.

AU - Huisman, T. A.G.M.

PY - 2009/3/1

Y1 - 2009/3/1

N2 - Sturge-Weber syndrome is a rare neurocutaneous disorder that typically presents with angiomas involving the face, ocular choroid and ipsilateral supratentorial leptomeninges. Posterior fossa involvement is extremely rare. We present two patients with simultaneous supra- and infratentorial involvement. Magnetic resonance imaging (MRI) and digital subtracted angiography (DSA) findings are discussed.

AB - Sturge-Weber syndrome is a rare neurocutaneous disorder that typically presents with angiomas involving the face, ocular choroid and ipsilateral supratentorial leptomeninges. Posterior fossa involvement is extremely rare. We present two patients with simultaneous supra- and infratentorial involvement. Magnetic resonance imaging (MRI) and digital subtracted angiography (DSA) findings are discussed.

KW - Cerebral conventional angiography

KW - Magnetic resonance imaging (MRI)

KW - Sturge-Weber syndrome

UR - http://www.scopus.com/inward/record.url?scp=61849146247&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=61849146247&partnerID=8YFLogxK

U2 - 10.1016/j.neurad.2008.07.008

DO - 10.1016/j.neurad.2008.07.008

M3 - Article

C2 - 18722014

AN - SCOPUS:61849146247

SN - 0150-9861

VL - 36

SP - 57

EP - 60

JO - Journal of Neuroradiology

JF - Journal of Neuroradiology

IS - 1

ER -

Sturge-Weber syndrome with cerebellar involvement

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this