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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… 
National Institutes of Health

Papers overview

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2012
2012
Muenke syndrome is characterized by various craniofacial deformities and is caused by an autosomal-dominant activating mutation… 
2011
2011
Parker's model is one of the most discussed mechanisms for coronal heating and has generated much debate. We have recently… 
Review
2009
Review
2009
An overview of Kuwaiti Arabic is presented, with very preliminary data from two typically developing brothers (ages 2;4 and 5;2… 
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… 
Review
2005
Review
2005
Characteristic deformities of skull shape occur as a result of different patterns of sutural fusion, while compen- satory skull… 
2004
2004
A comprehensive case and statistical study of CME onsets has been conducted on the solar limb using the CDS, LASCO and EIT… 
1996
1996
Study Design. Frontal plane geometry of postoperative curves was analyzed using a geometric model to investigate the relationship…