Abstract
Noonan syndrome is characterised by distinct facial stigmata, short stature and congenital cardiopathy. It has a high genetic heterogeneity and mutations in six different genes can be involved. We report a patient with Noonan syndrome and a novel KRAS mutation who presents systemic lupus erythematosus.
MeSH terms
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Adolescent
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Comorbidity
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Female
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Genetic Predisposition to Disease / genetics
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Humans
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Lupus Erythematosus, Systemic / diagnosis
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Lupus Erythematosus, Systemic / epidemiology*
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Lupus Erythematosus, Systemic / genetics*
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Mutation / genetics*
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Noonan Syndrome / diagnosis
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Noonan Syndrome / epidemiology*
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Noonan Syndrome / genetics*
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Proto-Oncogene Proteins / genetics*
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Proto-Oncogene Proteins p21(ras)
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ras Proteins / genetics*
Substances
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KRAS protein, human
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Proto-Oncogene Proteins
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Proto-Oncogene Proteins p21(ras)
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ras Proteins