Treatment Methods for Infant Encephalitis and Brain Atrophy

An infant of seven months was diagnosed with encephalitis, with a course of illness lasting for one and a half months. The condition involved genetic metabolic diseases, accompanied by bilateral thalamic and frontal-temporal softening foci, as well as brain atrophy. Additionally, there were also observations of brain fissure abnormalities in the posterior part of both frontal lobes and inflammation in both mastoids.
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Treatment Methods for Pediatric Adenoid Hypertrophy

After a child’s cold subsides, two small white spots are found on the tonsils, and during afternoon naps, the child breathes through the mouth due to nasal congestion. A visit to the otorhinolaryngology department results in a diagnosis of adenoid hypertrophy with concurrent rhinitis. Despite taking ceftriaxone, azithromycin, Balanophylla oral liquid, and ambroxol oral solution, the white spots have not receded. What should be done?
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