Pontine tegmental cap dysplasia with a duplicated internal auditory canal
نویسندگان
چکیده
منابع مشابه
Cochlear implantation in pontine tegmental cap dysplasia.
Pontine tegmental cap dysplasia (PTCD) is an exceptionally rare brain stem and cerebellar malformation characterized by ventral pontine hypoplasia, vaulted pontine tegmentum, hypoplasia of the vermis, subtotal absence of middle cerebellar peduncles, lateralized course of the superior cerebellar peduncles, and absence or alteration of the inferior olivary nucleus. The main clinical features are ...
متن کاملPontine tegmental cap dysplasia: the neurotologic perspective.
OBJECTIVES Pontine tegmental cap dysplasia (PTCD) is a rare congenital malformation. Clinical and imaging findings in 3 patients and the authors' experience with bilateral cochlear implantation in 1 patient are described. STUDY DESIGN Retrospective review. SETTING Two tertiary medical centers. SUBJECTS AND METHODS Three patients were evaluated by an otolaryngologist and underwent magnetic...
متن کاملNovel clinical features in pontine tegmental cap dysplasia.
Pontine tegmental cap dysplasia is a rare neurologic condition first described by Barth et al. in 2007. It is characterized by a vaulted pontine tegmentum projecting into the fourth ventricle and ventral pontine hypoplasia. Patients present with developmental delay, cerebellar and pyramidal abnormalities, cranial nerve dysfunction, and various extracranial malformations. The condition is though...
متن کاملPontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance.
Four unrelated children are described with an identical brainstem and cerebellar malformation on MRI. The key findings are: vermal hypoplasia, subtotal absence of middle cerebellar peduncles, flattened ventral pons, vaulted pontine tegmentum, molar tooth aspect of the pontomesencephalic junction and absent inferior olivary prominence. Peripheral hearing impairment is present in all. Variable fi...
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ژورنال
عنوان ژورنال: Radiology Case Reports
سال: 2019
ISSN: 1930-0433
DOI: 10.1016/j.radcr.2019.04.009