Syndrome in question

Abstract

Ross syndrome is a rare disease characterized by peripheral nervous system dysautonomia with selective degeneration of cholinergic fibers. It is composed by the triad of unilateral or bilateral segmental anhidrosis, deep hyporeflexia and Holmes-Adie's tonic pupil. The presence of compensatory sweating is frequent, usually the symptom that most afflicts patients. The aspects of the syndrome are put to discussion due to the case of a male patient, caucasian, 47 years old, with clinical onset of 25 years.

Adie pupil. Literature review

“…Neu ro lo gi nio ið ty ri mo me tu svar bu at kreip ti dë me sá á gi liuo sius saus gys liø re flek sus -esant jø su sil pnë ji mui ar ið ny ki mui, diag no zuo ja mas Adie sin dro mas [4,15,21]. Áver ti nus re flek sus, ti ria ma dël seg men ti nio su ma þë ju sio pra kai ta vi mo vie no je ar abie jo se pu së se, no rint at mes ti Ross sin dro mà [4,34].…”