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Article

Fibrillin-1 gene analysis of Korean patients with spontaneous CSF hypovolemia.

Headache - 1 Jan 2007

Chung Sun J, Ki Chang-Seok, Lee Myoung C, Lee Jae-Hong

Abstract excerpt

BACKGROUND: Mutations in different domains of the Fibrillin-1 (FBN1) gene may be responsible for the variable phenotypic expression of Marfan's syndrome that may present with CSF hypovolemia. OBJECTIVES: To evaluate the association between mutations in the Fibrillin-1 (FBN1) gene and spontaneous CSF hypovolemia (SCH) in a Korean population. METHODS: We studied 10 consecutive patients with SCH without clinical...

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Source

Identifiers

PMID: 17355504
DOI: 10.1111/j.1526-4610.2006.00635.x

Genes

FBN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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