Muenke Syndrome

Known as: Muenke nonsyndromic coronal craniosynostosis, FGFR3-Associated Coronal Synostosis, Syndrome of coronal craniosynostosis 
A rare autosomal dominant inherited disorder caused by mutations in the FGFR3 gene. It is characterized by premature fusion of cranial bones… (More)
National Institutes of Health

Papers overview

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2009
2009
The heterozygous Pro250Arg substitution mutation in fibroblast growth factor receptor 3 (FGFR3), which increases ligand-dependent… (More)
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2009
2009
Muenke syndrome (MS), also known as Muenke nonsyndromic coronal craniosynostosis, is an autosomal dominant condition which can be… (More)
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2007
2007
The purpose of this study was to test whether the severity of the cranial phenotype in Muenke syndrome infants with unicoronal… (More)
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Quantitative magnetic resonance imaging (qMRI) may provide valuable measures of cartilage morphology in osteoarthritis… (More)
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2006
2006
Saethre-Chotzen syndrome is caused by mutations in the TWIST gene on chromosome 7p21.2. However, Muenke et al. [(1997); Am J Hum… (More)
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Highly Cited
2005
Highly Cited
2005
STUDY DESIGN Retrospective study. OBJECTIVES To evaluate outcomes of selective thoracic fusion with segmental pedicle screw… (More)
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2003
2003
Hypochondroplasia (HCH) and Muenke syndrome (MS) are caused by mutations on FGFR3 gene. FGFR3 is known to play a role in… (More)
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1998
1998
An analysis is provided of the consonant harmony (CH) patterns exhibited in the speech of one child, Amahl at Stage 1 (data from… (More)
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Highly Cited
1991
Highly Cited
1991
From 1985 to 1987, 82 patients with idiopathic scoliosis followed 12 to 44 months underwent selective fusion and correction of… (More)
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