Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression
- 15 September 2011
- journal article
- case report
- Published by Springer Science and Business Media LLC in European Journal of Pediatrics
- Vol. 171 (3), 447-450
- https://doi.org/10.1007/s00431-011-1557-8
Abstract
No abstract availableKeywords
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- Diagnostic difficulties in lymphedema distichiasis.Pediatric Dermatology, 2003
- Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis SyndromeAmerican Journal of Human Genetics, 2000
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