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Moyamoya Disease, Which is Rare in Infancy: A Case Report

Moyamoya Disease, Which is Rare in Infancy: A Case Report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3198217806

Moyamoya Disease, Which is Rare in Infancy: A Case Report

About this item

Full title

Moyamoya Disease, Which is Rare in Infancy: A Case Report

Publisher

Istanbul: Galenos Publishing House

Journal title

Cocuk Acil ve Yogun Bakım, 2023-12, Vol.10 (3), p.224

Language

Formats

Publication information

Publisher

Istanbul: Galenos Publishing House

More information

Scope and Contents

Contents

[LANGUAGE=”English”]Moyamoya disease etiology is an undetermined vasculopathy and is mainly thought to affect the Internal Carotid Artery and Wills circle. An 8-month-old patient without any underlying disease was referred to our hospital with sudden extreme right hemiparesis. There was no evidence of meningeal irritation in the neurological examin...

Alternative Titles

Full title

Moyamoya Disease, Which is Rare in Infancy: A Case Report

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_3198217806

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3198217806

Other Identifiers

ISSN

2146-2399

E-ISSN

2717-9206

DOI

10.4274/cayd.galenos.2023.56933

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