夏皮罗综合征患者肉碱缺乏症

P. Yager, Maria Alkhasova, D. Rudy
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引用次数: 1

摘要

自发性多汗症伴低体温和胼胝体发育不全被称为经典夏皮罗综合征(CSS),由夏皮罗和梅在1967年首次报道。我们报告了一个有充分文献记载的病例,一名39岁的女性在5岁时被诊断为SS,她在30岁时被诊断为肉碱缺乏症。这是第一例报道的左旋肉碱缺乏症的SS,用左卡尼汀治疗。本例患者还伴有其他SS病例报告的合并症诊断,包括原发性闭经(未经治疗)、原发性甲状腺功能减退(用左甲状腺素和碘甲状腺原氨酸治疗)、癫痫发作(用拉莫三嗪、左乙拉西坦和醋酸埃斯卡巴西平治疗)和低温诱导的细胞减少(用碘甲状腺原氨酸治疗)。此外,本病例提供了从纵向护理中获得的独特见解。
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Carnitine Deficiency in a Patient with Shapiro Syndrome
Spontaneous hyperhidrosis with hypothermia and agenesis of the corpus callosum is known as Classical Shapiro Syndrome (CSS) and was first reported by Shapiro and Plum in 1967. We report a well-documented case of a 39-yearold woman with SS diagnosed at the age of 5-years-old who was diagnosed with Carnitine deficiency at 30-years-old. This is the first reported case of SS with Carnitine deficiency, which was treated with levocarnitine. Our patient also carries with her several comorbid diagnoses which have been reported in other cases of SS. These include primary amenorrhea (untreated), primary hypothyroidism (treated with levothyroxine and liothyronine), seizure disorder (treated with lamotrigine, levetiracetam, and eslicarbazepine acetates), and hypothermia-induced cytopenia (resolved with the addition of liothyronine). Additionally, this case offers unique insights gained from longitudinal care.
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