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題名 | Setleis Syndrome--Bitemporal “Forceps Marks” Syndrome in a 6-day-old Taiwanese Infant=Setleis徵候群於六天大之臺灣嬰兒--病例報告 |
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作者姓名(中文) | 魏楷哲; 李玉雲; 林秀娟; | 書刊名 | 中華皮膚科醫學雜誌 |
卷期 | 24:4 民95.12 |
頁次 | 頁266-268 |
分類號 | 417.509 |
關鍵詞 | Setleis氏徵候群; 先天性表皮發育不全; Bitemporal forceps marks; Atrophic scar; Setleis syndrome; Aplasia cutis congenita; |
語文 | 英文(English) |
中文摘要 | Setleis氏徵候群,是種少見的先天性表皮發育不全;臨床上,兩側顳部有類似產鉗夾傷的疤痕,合併異常傾斜的眉毛、部分睫毛缺損、前額髮線較低及噘起的嘴型。我們報告第一例台灣的Setleis氏徵候群,並整理相關的文獻:一個台灣出生,六天大的男嬰,雙親非近親結婚且外觀正常,發現兩側顳部有萎縮、類似疤痕的斑塊,傾斜的眉毛、部分睫毛缺損,沒有合併其他的發育異常;追蹤六個月後,前額髮線較低及噘起的嘴型變得益發明顯,但生長、發育都正常。 |
英文摘要 | Setleis syndrome, a variant of aplasia cutis congenita, is a rare genetic disease characterized by bitemporal scarring resembling forceps marks, abnormal eyebrows and eyelashes, low frontal hairline and 'pursed lips'. We report the first Taiwanese case in a 6-day-old full-term male infant who was born spontaneously to unrelated, normal-appearing parents with atrophic scar-like lesions on the bilateral temporal areas. In addition, upward slanting of the eyebrows and partial absence of the lateral brows were found. There were no other obvious development anomalies. Low frontal hair line and 'pursed lips' appearance became more apparent at 6-month of age. The baby was otherwise normal, alert and active. The clinical features are consistent with Setleis syndrome. |
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