Hearing loss and middle ear disorders patients with Down's syndrome (mongolism).
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Biomedical subjects
Publications and source records attributed to G C Kanjilal.
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Two cases of `spontaneous cerebral ventriculostium' are reported. In one case the diagnosis was made during life, and the hydrocephalus was not relieved by the ostium. The unique feature of the other has been the presence of a large defect in the skull bones, posteriorly, which has been a `nature's help' towards maintaining the hydrocephalus stationary, after an initial period of progression.
The clinical features in a new non-familial case of Cockayne's syndrome comprised the usual components: dwarfism with microcephaly, severe mental subnormality, progeria-like appearance of the face, pigmented retinopathy, and severe perceptive deafness. The patient also suffered from grand mal epilepsy and died in status epilepticus at the age of 22 years. The neuropathological findings were severe microencephaly, widespread calcifying vasopathy with some secondary degenerative changes in the contiguous tissue, and granular ependymitis.
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