X-Linked Stapes Gusher: CT Findings in One Patient

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Summary: A 31-year-old male patient presented with progressive mixed hearing loss since birth. A stapedectomy was attempted and was unsuccessful because of perilymph gushing. CT of the temporal bones showed bulbous dilatation of the fundi of the internal auditory canals and absence of the bone plates separating them from the base of the cochleas. This unusual abnormality was found after the attempted stapedectomy and explains the clinical findings. The findings in male patients are fairly typical X-linked congenital deafness.
X-Linked Stapes Gusher: CT Findings in One Patient
Figure 2 from CT and MRI findings in X-linked progressive deafness.
X-Linked Stapes Gusher: CT Findings in One Patient
EPOS™
X-Linked Stapes Gusher: CT Findings in One Patient
Axial 3D T2WI in a male patient with X-linked deafness with mixed
X-Linked Stapes Gusher: CT Findings in One Patient
Brazilian Society of Otology task force – Otosclerosis: evaluation and treatment
X-Linked Stapes Gusher: CT Findings in One Patient
Brazilian Society of Otology task force – Otosclerosis: evaluation and treatment
X-Linked Stapes Gusher: CT Findings in One Patient
A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations
X-Linked Stapes Gusher: CT Findings in One Patient
X-linked mixed hearing loss in a young boy with developmental delay and
X-Linked Stapes Gusher: CT Findings in One Patient
Genes, Free Full-Text
X-Linked Stapes Gusher: CT Findings in One Patient
X-Linked Progressive Mixed Hearing Loss: Computed Tomography Findings - Alan Tang, Lorne S. Parnes, 1994
X-Linked Stapes Gusher: CT Findings in One Patient
Brothers with X-linked congenital hearing loss
X-Linked Stapes Gusher: CT Findings in One Patient
PDF) X-linked stapes gusher: CT findings in one patient
X-Linked Stapes Gusher: CT Findings in One Patient
X-linked congenital deafness
X-Linked Stapes Gusher: CT Findings in One Patient
Frontiers Novel POU3F4 variants identified in patients with inner ear malformations exhibit aberrant cellular distribution and lack of SLC6A20 transcriptional upregulation
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