Das somatische infantile kapilläre Hämangiom ist ein häufiger bei Neugeborenen und Kleinkindern gefundener benigner rötlicher Hauttumor. In den Tumoren finden sich somatische Mutationen in den Genen FLT4 und KDR.
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1. |
Walter JW et al. (2002) Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma. ![]() |
2. |
Blei F et al. (1998) Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait. ![]() |
3. |
Walter JW et al. (1999) Genetic mapping of a novel familial form of infantile hemangioma. ![]() |
4. |
Breugem CC et al. (2002) A locus for hereditary capillary malformations mapped on chromosome 5q. ![]() |
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. ![]() |
6. |
Waner M et al. (2003) The nonrandom distribution of facial hemangiomas. ![]() |
7. |
Spring MA et al. (2005) Cutaneous vascular lesions. ![]() |
8. |
Pramanik K et al. (2009) Dusp-5 and Snrk-1 coordinately function during vascular development and disease. ![]() |
9. |
Jinnin M et al. (2008) Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma. ![]() |
10. |
OMIM.ORG article Omim 602089![]() |