Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Familial infantile capillary hemangioma is a common benign red skin tumor in newborns and infants. Inheritance is autosomal dominant. The disease is caused by mutations of the ANTXR1 and KDR genes.
Capillary infantile hemangioma
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Capillary infantile hemangioma
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Capillary infantile hemangioma with germline mutation
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FLT4
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FLT4
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| 1. |
Walter JW et al. (2002) Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma. 
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| 2. |
Blei F et al. (1998) Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait.
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| 3. |
Walter JW et al. (1999) Genetic mapping of a novel familial form of infantile hemangioma.
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| 4. |
Breugem CC et al. (2002) A locus for hereditary capillary malformations mapped on chromosome 5q.
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| 5. |
Ritter MR et al. (2002) Insulin-like growth factor 2 and potential regulators of hemangioma growth and involution identified by large-scale expression analysis.
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| 6. |
Waner M et al. (2003) The nonrandom distribution of facial hemangiomas.
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| 7. |
Spring MA et al. (2005) Cutaneous vascular lesions.
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| 8. |
Pramanik K et al. (2009) Dusp-5 and Snrk-1 coordinately function during vascular development and disease.
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| 9. |
Jinnin M et al. (2008) Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.
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| 10. |
OMIM.ORG article Omim 602089
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