A GIRL WITH STURGE WEBER SYNDROME AND ORO -MAXILLO -FACIAL OSTEODYSTROPHY

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

AHMADIPOUR SHOKOOFEH; MOHSENZADEH AZAM; BABAEI HOMA

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Yafteh Year:2014 | Volume:16 | Issue:3 (61) Page(s): 112-117

Download Full-Text

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

View:

1,462

Download:

Cites:

Information Journal Paper

Title

A GIRL WITH STURGE WEBER SYNDROME AND ORO -MAXILLO -FACIAL OSTEODYSTROPHY

Author(s)

AHMADIPOUR SHOKOOFEH | MOHSENZADEH AZAM | BABAEI HOMA | Issue Writer Certificate

Keywords

SYNDROMEQ3

STURGEQ2

WEBERQ3

SEIZUREQ2

OSTEODYSTROPHYQ2

Abstract

Background: STURGE-Weber SYNDROME is one of the rare neurocutaneous disorders with frequency of approximately 1 per 50,000. STURGE-Weber SYNDROME consists of a constellation of symptoms and signs including a facial nevus (port wine stain), SEIZURE and hemiparesis. In many cases it may associate with mental retardation.Case presentation: A 7- year old girl with mental retardation and a large facial nevus at the birth time, recurrent severe SEIZUREs and drolling in 9 months of life without any treatment, was admitted because of severity of SEIZURE, headache and weakness. Conducted follow up on here, indicated that she had STURGE-Weber SYNDROME with oro- maxilla -facial OSTEODYSTROPHY.Conclusion: One of the rare radiological symptoms in STURGE WEBER SYNDROME is oro-maxillo-facial OSTEODYSTROPHY, by this time only few cases had been reported. All of the symptoms of this SYNDROME were found in our described patient.

Cites

No record.

References

No record.

Cite

APA: Copy

AHMADIPOUR, SHOKOOFEH, MOHSENZADEH, AZAM, & BABAEI, HOMA. (2014). A GIRL WITH STURGE WEBER SYNDROME AND ORO -MAXILLO -FACIAL OSTEODYSTROPHY. YAFTEH, 16(3 (61)), 112-117. SID. https://sid.ir/paper/79981/en

Vancouver: Copy

AHMADIPOUR SHOKOOFEH, MOHSENZADEH AZAM, BABAEI HOMA. A GIRL WITH STURGE WEBER SYNDROME AND ORO -MAXILLO -FACIAL OSTEODYSTROPHY. YAFTEH[Internet]. 2014;16(3 (61)):112-117. Available from: https://sid.ir/paper/79981/en

IEEE: Copy

SHOKOOFEH AHMADIPOUR, AZAM MOHSENZADEH, and HOMA BABAEI, “A GIRL WITH STURGE WEBER SYNDROME AND ORO -MAXILLO -FACIAL OSTEODYSTROPHY,” YAFTEH, vol. 16, no. 3 (61), pp. 112–117, 2014, [Online]. Available: https://sid.ir/paper/79981/en

Related Journal Papers