Molybdenum Cofactor Deficiency

W. Nyhan
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Abstract

Molybdenum cofactor deficiency is a rare condition characterized by brain dysfunction (encephalopathy) that worsens over time. Babies with this condition appear normal at birth, but within a week they have difficulty feeding and develop seizures that do not improve with treatment (intractable seizures). Brain abnormalities, including deterioration (atrophy) of brain tissue, lead to severe developmental delay; affected individuals usually do not learn to sit unassisted or to speak. A small percentage of affected individuals have an exaggerated startle reaction (hyperekplexia) to unexpected stimuli such as loud noises. Other features of molybdenum cofactor deficiency can include a small head size (microcephaly) and facial features that are described as "coarse."
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缺钼辅助因子
钼辅助因子缺乏症是一种罕见的以脑功能障碍(脑病)为特征的疾病,随着时间的推移而恶化。患有这种疾病的婴儿在出生时看起来很正常,但在一周内,他们就会出现进食困难,并出现癫痫发作,这种症状得不到治疗(顽固性癫痫发作)。大脑异常,包括脑组织恶化(萎缩),导致严重的发育迟缓;受影响的人通常无法学会独自坐着或说话。一小部分受影响的人对意外的刺激(如大声的噪音)有夸张的惊吓反应(过度兴奋症)。钼辅助因子缺乏的其他特征包括头小(小头畸形)和面部特征被描述为“粗糙”。
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