According to the definition by American Academy of Family Physicians, Clinical practice guidelines are statements that include recommendations intended to optimize patient care. The National Institute for Health and Care Excellence (NICE) is a non-departmental public body in England, that provides national guidance and advice to improve health and social care. On 7th March 2019, […]
A 12 year old male child was referred from pediatric department following resolution of third episode of meningitis, with complaints of left side hearing loss since childhood. Parents noticed the hearing loss on left side when the child was in fourth standard. No newborn hearing screening was done for the child at birth. Investigations Blood / […]
Inner ear malformations (IEM) represent about 20%–35% of the etiology of congenital sensorineural hearing loss (SNHL). Incomplete cochlear partition anomalies characterize a group of IEM with normal cochlear location, external dimensions (height and length) but with various internal architecture defects. In these collections of malformations, there is a clear distinction into a cochlea and vestibule. […]
Cochlear implants are electronic prosthetic devices used in adults and children with sensory neural hearing loss, who are not benefited by the use of conventional hearing aids. They bypasses the functions of damaged hair cells inside the inner ear and directly stimulates the spiral ganglion of cochlear nerve (nerve of hearing).
Cochlear Implant (CI) is a prosthetic electronic device which replaces the function of damaged inner ear. CI provides direct electrical stimulation to the auditory (hearing) nerve in the inner ear bypassing the damaged hair cells. They are used in patients (both adults and children) with sensory neural hearing loss who are not benefited by conventional hearing aids. […]
Incomplete Partition type III (IP-III) or most widely known as X linked deafness is an inner ear anomaly associated with congenital mixed hearing loss, fixation of stapes footplate and perilymph gusher during stapes or cochlear implant surgery . Phippard addressed this anomaly as pseudo-Mondini stage II and described as partial hypoplasia of the cochlea, stapes fixation, dilated […]