Cutis Gyrata Syndrome of Beare And Stevenson

Known as: Beare-Stevenson Cutis Gyrata Syndrome, Cutis Gyrata Syndrome of Beare-Stevenson, BEARE-STEVENSON SYNDROME 
A rare, autosomal dominant inherited disorder caused by mutations in the FGFR2 gene. It is characterized by the premature fusion of the bones of the… (More)
National Institutes of Health

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Topic mentions per year

1964-2016
02419642016

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2016
2016
Aplasia cutis congenita of the scalp (ACCS) is a rare congenital disease.1–3 The exact prevalence is still unknown. It was first… (More)
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2016
2016
INTRODUCTION Cutis verticis gyrata is a rare skin disorder characterized by formation of thick skin folds and grooves. Because of… (More)
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2016
2016
Aplasia Cutis Congenita (ACC) is a condition characterized by congenital absence of skin, usually on the scalp. ACC can occur as… (More)
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Review
2003
Review
2003
Premature fusion of cranial sutures underlies the clinical condition of 'craniosynostosis', a common human disorder that occurs… (More)
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2002
2002
The patient was a male baby who was born after a full-term pregnancy. His mother was 31 years old and his father was 34 years old… (More)
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2000
2000
Cutis verticis gyrata (CVG) is a rare disorder; it is characterized by thickening of the scalp which becomes raised to form… (More)
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1998
1998
The clinical and radiological features of a patient with Cutis Verticis Gyrata-Mental Deficiency syndrome are reported. The… (More)
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1981
1981
A case of so-called, "Pseudo"-Cutis verticis gyrata naevocellularis is described. The possible malignant degeneration of this… (More)
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