先天性中线头皮和颅骨缺损。
Congenital midline scalp and skull defect.
作者信息
Lassman L P, Sims D G
出版信息
Arch Dis Child. 1975 Dec;50(12):958-60. doi: 10.1136/adc.50.12.958.
Abstract
A family with multiple congenital scalp defects, over two generations and probably genetically determined, is described. Although alarming in appearance, surgical intervention is not indicated at least for small lesions. The risk of haemorrhage and meningitis is emphasized.
摘要
本文描述了一个有两代人患有多发性先天性头皮缺损的家族，可能由基因决定。尽管外观令人担忧，但至少对于小病变，不建议进行手术干预。文中强调了出血和脑膜炎的风险。
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本文引用的文献
1
CONGENITAL SCALP DEFECTS IN FATHER AND SON.父子先天性头皮缺损
Am J Dis Child. 1965 Sep;110:297-8. doi: 10.1001/archpedi.1965.02090030311014.
2
CONGENITAL SCALP DEFECTS IN TWIN SISTERS.双胞胎姐妹的先天性头皮缺损
Am J Dis Child. 1965 Sep;110:293-5. doi: 10.1001/archpedi.1965.02090030307013.
3
Familial congenital defect of the scalp.
AMA Arch Derm. 1957 Feb;75(2):266-7. doi: 10.1001/archderm.1957.01550140110020.
4
Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.一名患有中线融合缺陷儿童的4号至5号染色体短臂缺失。
Humangenetik. 1965;1(5):479-82. doi: 10.1007/BF00279124.
5
Congenital defects of the scalp. A surgical approach to aplasia cutis congenita.头皮先天性缺陷。先天性皮肤发育不全的手术治疗方法。
J Neurosurg. 1970 Aug;33(2):198-202. doi: 10.3171/jns.1970.33.2.0198.
6
Congenital scalp defects: aplasia cutis congenita.先天性头皮缺损：先天性皮肤发育不全
J Neurosurg. 1975 Jan;42(1):32-6. doi: 10.3171/jns.1975.42.1.0032.
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