WordNet

of or relating to the sympathetic nervous system; "sympathetic neurons"; "sympathetic stimulation"
(of characters in literature or drama) evoking empathic or sympathetic feelings; "the sympathetic characters in the play" (同)appealing, likeable, likable
expressing or feeling or resulting from sympathy or compassion or friendly fellow feelings; disposed toward; "sympathetic to the students cause"; "a sympathetic observer"; "a sympathetic gesture"
having similar disposition and tastes; "with their many similar tastes, he found her a most sympathetic companion"

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1. 神経芽細胞腫の臨床所見、診断、および病期分類評価 clinical presentation diagnosis and staging evaluation of neuroblastoma
2. ホルネル症候群 horner syndrome
3. 瞳孔不同患者へのアプローチ approach to the patient with anisocoria
4. スタージウェーバー症候群 sturge weber syndrome
5. 網膜芽細胞腫：臨床症状、評価、診断 retinoblastoma clinical presentation evaluation and diagnosis

Marín-Lambíes C1, España-Gegori E, Gallego-Pinazo R, Climent-Vallano L, Muelas N, Díaz-Llopis M.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.J Neuroophthalmol.2012 Dec;32(4):348-9. doi: 10.1097/WNO.0b013e3182625212.
Pourfour du Petit syndrome is a rare dysautonomic disorder characterized by mydriasis, eyelid retraction, and hyperhidrosis and is caused by irritative stimulation of the sympathetic cervical chain. The authors describe a 45-year-old woman with iris heterochromia, who presented with episodes of ipsi
PMID 22801354

Wang FM1, Wertenbaker C, Cho H, Marmor MA, Ahn-Lee SS, Bernard BA.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.J Neuroophthalmol.2012 Jun;32(2):132-4. doi: 10.1097/WNO.0b013e318240c678.
Congenital Horner syndrome is a rare disorder that accounts for less than 5% of all cases of Horner syndrome. Like Horner syndrome in general, it consists primarily of ptosis, miosis, and anhidrosis. Congenital Horner syndrome may manifest some special features such as iris heterochromia since the s
PMID 22622362

Congenital agenesis of internal carotid artery with ipsilateral Horner presenting as focal neurological symptoms.

Farhat W1, Ahdab R, Hosseini H.
Vascular health and risk management.Vasc Health Risk Manag.2011 Jan 26;7:37-40. doi: 10.2147/VHRM.S16642.
Internal carotid artery (ICA) agenesis is a rare developmental anomaly and is most frequently asymptomatic, but it may also present as cerebrovascular accidents. The association with Horner's syndrome is exceptional. We present three cases of agenesis of ICA associated with Horner's syndrome and hyp
PMID 21339912