Multiple lentigines

Presence of an unusually high number of lentigines (singular: lentigo), which are flat, tan to brown oval spots. [HPO:probinson]
National Institutes of Health

Papers overview

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Review
2013
Review
2013
The RASopathies are a clinically defined group of medical genetic syndromes caused by germline mutations in genes that encode… (More)
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Highly Cited
2010
Highly Cited
2010
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous developmental disorder… (More)
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Review
2008
Review
2008
LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainly characterized by skin, facial and… (More)
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2004
2004
Noonan (NS) and multiple lentigines/LEOPARD syndromes (LS) have proved to be associated with distinct PTPN11 mutations. Noonan… (More)
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Highly Cited
2003
Highly Cited
2003
N oonan syndrome (MIM 163950), an autosomal dominant disorder with an estimated prevalence of 1/1000– 2500 at birth, is… (More)
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Highly Cited
2002
Highly Cited
2002
Multiple-lentigines (ML)/LEOPARD (multiple lentigines, electrocardiographic-conduction abnormalities, ocular hypertelorism… (More)
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Highly Cited
2002
Highly Cited
2002
LEOPARD syndrome is an autosomal dominant disorder with multiple lentigines, congenital cardiac abnormalities, ocular… (More)
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1997
1997
The multiple lentigines syndrome is an autosomal dominant condition which has many similarities to Noonan syndrome, except in the… (More)
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1992
1992
Forty-one children, ranging in age from 1 month to 14 years, had six or more café au lait spots at their initial visit and were… (More)
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1971
1971
The Leopard syndrome, an acronym, consists of the following features: L-lentigines (multiple), E-electrocardiographic… (More)
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