Atypical Craniosynostosis with Torticollis and Neurological Symptoms: A Rhombencephalosynapsis Sequence
نویسندگان
چکیده
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. Therefore, we conclude that patients with atypical craniosynostosis should be examined with brain-MRI to exclude the intracranial malformations, which 3D-CT does not reveal. Without brain-MRI, decision (not) to perform surgery could have been different.
منابع مشابه
Rhombencephalosynapsis: new findings in a larger study.
Rhombencephalosynapsis: new findings in a larger study Rhombencephalosynapsis is a developmental midline defect affecting the cerebellar vermis. The absence of the vermis in rhomben-cephalosynapsis may be compared to the other condition in which the vermis is largely absent. In Joubert syndrome, the cerebellar hemispheres are close to normal in volume; the intervening vermis is small and much s...
متن کاملCongenital Muscular Torticollis Concurrent With Sagittal Synostosis: A Case Report
Congenital muscular torticollis (CMT) and craniosynostosis are diseases that cause plagiocephaly and craniofacial asymmetry in children. In our literature review, we did not find any report of concurrent manifestation of CMT and craniosynostosis. A 41-month-old boy visited our hospital with left torticollis, right laterocollis, and craniofacial asymmetry as the main findings. During clinical ex...
متن کاملRhombencephalosynapsis: A Rare Cerebellar Malformation
Background: Rhombencephalosynapsis is characterized by agenesis/hypogenesis of the cerebellar vermis along with the fusion of the cerebellar hemispheres in the midline. There are less than 50 cases in the literature, and adult cases are extremely rare. In this paper, an adult patient with rhombencephalosynapsis is reported. Case: A 24-year-old female was admitted with the complaint of headache....
متن کاملRhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity.
Rhombencephalosynapsis is a midline brain malformation characterized by missing cerebellar vermis with apparent fusion of the cerebellar hemispheres. Rhombencephalosynapsis can be seen in isolation or together with other central nervous system and extra-central nervous system malformations. Gómez-López-Hernández syndrome combines rhombencephalosynapsis with parietal/temporal alopecia and someti...
متن کاملTo spasm , or Not to Spasm , That is the Question Case Report
Introduction Typically, cervical dystonia (CD), or spasmodic torticollis, is described as a condition in which the cervical paraspinal muscle groups in the neck undergo uncontrollable and prolonged spasm. It has been well described in the literature that CD presents in most patients with an extreme head tilt or tremor due to spasm. This has become the all-encompassing definition of CD to many c...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 2009 شماره
صفحات -
تاریخ انتشار 2009