Purpose. We describe a case of 3-year-old girl with rhombencephalosynapsis, a rare cerebellar anomaly. Patient. A 3-year-old girl was admitted to our hospital due to congenital torticollis and asymmetry of face, skull and trunk. Craniosynostosis was suspected due to abnormal head shape. 3D-CT revealed closure of the sagittal suture without scaphocephalic skull. Due to atypical craniosynostosis with neurological symptoms, brain-MRI was performed revealing rhombencephalosynapsis. Results. Our patient presented with atypical craniosynostosis and balance problems, not typical for scaphocephaly. Operative treatment for craniosynotosis was not carried out because the cause of the problems was the cerebellum instead of the brain. Conclusions. The...
International audienceRhombencephalosynapsis is an uncommon cerebellar malformation defined by vermi...
The incidence of congenital torticollis in association with plagiocephaly is 1 in 300 newborns, with...
We present the case of a preterm 6-month-old African American infant who developed craniosynostosis ...
Background: Rhombencephalosynapsis (RES) is a rare malformation of the posterior cranial fossa, char...
An unusual disorder of cerebellar development, rhombencephalosynapsis is a unique entity which prese...
Rhombencephalosynapsis is a rare congenital abnormality characterised by dorsal fusion of the cerebe...
Congenital muscular torticollis (CMT) and craniosynostosis are diseases that cause plagiocephaly and...
Abstract Rhombencephalosynapsis is a rare cerebellar malformation. It is characterised by dorsal fus...
Background: Rhombencephalosynapsis (RES) is a rare malformation of the posterior cranial fossa, char...
Background: Rhomboencephalosynapsis (RES, RS) is a unique entity usually recognized in infancy based...
An unusual disorder of cerebellar development, rhombencephalosynapsis is a unique entity which prese...
WOS: 000087736300009PubMed ID: 10842053Rhombencephalosynapsis is mainly characterized by fusion of t...
The clinical and MRI findings in two cases of rhombencephalosynapsis (RS) and two of tectocerebellar...
Pseudotumor cerebri syndrome is an uncommon disease in children. It’s on time diagnosis and treatmen...
Although the need to prevent the secondary effects of craniosynostosis on the central nervous system...
International audienceRhombencephalosynapsis is an uncommon cerebellar malformation defined by vermi...
The incidence of congenital torticollis in association with plagiocephaly is 1 in 300 newborns, with...
We present the case of a preterm 6-month-old African American infant who developed craniosynostosis ...
Background: Rhombencephalosynapsis (RES) is a rare malformation of the posterior cranial fossa, char...
An unusual disorder of cerebellar development, rhombencephalosynapsis is a unique entity which prese...
Rhombencephalosynapsis is a rare congenital abnormality characterised by dorsal fusion of the cerebe...
Congenital muscular torticollis (CMT) and craniosynostosis are diseases that cause plagiocephaly and...
Abstract Rhombencephalosynapsis is a rare cerebellar malformation. It is characterised by dorsal fus...
Background: Rhombencephalosynapsis (RES) is a rare malformation of the posterior cranial fossa, char...
Background: Rhomboencephalosynapsis (RES, RS) is a unique entity usually recognized in infancy based...
An unusual disorder of cerebellar development, rhombencephalosynapsis is a unique entity which prese...
WOS: 000087736300009PubMed ID: 10842053Rhombencephalosynapsis is mainly characterized by fusion of t...
The clinical and MRI findings in two cases of rhombencephalosynapsis (RS) and two of tectocerebellar...
Pseudotumor cerebri syndrome is an uncommon disease in children. It’s on time diagnosis and treatmen...
Although the need to prevent the secondary effects of craniosynostosis on the central nervous system...
International audienceRhombencephalosynapsis is an uncommon cerebellar malformation defined by vermi...
The incidence of congenital torticollis in association with plagiocephaly is 1 in 300 newborns, with...
We present the case of a preterm 6-month-old African American infant who developed craniosynostosis ...