Results 101 to 110 of about 3,158 (217)

Use physical therapy to head off this deformity in infants [PDF]

, 2009
Identify infants with positional preference early and consider referral to pediatric physical therapy at 7 or 8 weeks to prevent severe deformational plagiocephaly (DP).
Ewigman, Bernard, Hickner, John, Mendoza, Michael D., Vargish, Lisa   +3 more
core  

Gorlin-Goltz syndrome : Clinicopathologic aspects [PDF]

, 2008
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a genetic alteration produced by a mutation in the ?Patched?
Acha Sagredo, Amelia, Aguirre Urízar, José Manuel, García Arregui, Olatz, Ortega García de Amezaga, Aitziber, Zepeda Nuño, Sergio   +4 more
core  

A rare case of Muenke syndrome from The Gambia: a case report

Journal of Rare Diseases
Introduction Muenke syndrome is a form of syndromic craniosynostosis caused by a specific mutation in the FGFR3 gene. It is characterized by premature fusion of the coronal sutures, resulting in craniofacial abnormalities, hearing impairment, and ...
M. Bah, J. Barry, I. Bahoum, A. Jallow, S. Bah, A. Cham, L. Makalo   +6 more
doaj   +1 more source

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice [PDF]

, 2010
Yingli Wang, Miao Sun, Victoria L Uhlhorn, Xueyan Zhou, Inga Peter, Neus Martinez-Abadias, Cheryl A Hill, Christopher J Percival, Joan T Richtsmeier, David L Huso, Ethylin Jabs   +10 more
core   +1 more source

Brain and ventricular volume in patients with syndromic and complex craniosynostosis [PDF]

, 2011
T. de Jong, B. F. M. Rijken, M. H. Lequin, M. L. C. van Veelen, I. M. J. Mathijssen   +4 more
core   +1 more source

Unilateral craniosynostosis associated with ZIC1 gene mutation: a case report. [PDF]

J Surg Case Rep
Alsharef FK, Alraddadi KK, Aljared T.
europepmc   +1 more source

Neurocognitive outcomes in children with craniosynostosis after surgical correction: a narrative review. [PDF]

Ann Med Surg (Lond)
Wijdan SA, Yezdan SA, Asim R, Sakrani RA, Batool R, Abdalla MI.   +5 more
europepmc   +1 more source

Prenatal diagnosis of craniosynostosis: a case description and genetic evaluation. [PDF]

Quant Imaging Med Surg
Tang ZF, Lin XJ, Deng L, Yang T, Yang L.
europepmc   +1 more source

Sagittal craniosynostosis with Moebius syndrome; case illustration: first case in the literatüre. [PDF]

BMC Pediatr
Kuzucu P, Kale A, Asadov İ, Börcek AÖ.   +3 more
europepmc   +1 more source

Isolated frontosphenoidal craniosynostosis with pathogenic <i>FGFR3</i> variant: a case report and genetic insights. [PDF]

Transl Pediatr
Wei J, Liu B, Gao B, Liu M, Ni Z, Wang J, Wang X.   +6 more
europepmc   +1 more source