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首页> 外文期刊>Clinical dysmorphology >The fetal mycophenolate mofetil syndrome.
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The fetal mycophenolate mofetil syndrome.

机译:胎儿霉酚酸酯代谢综合征。

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Hypertelorism, epicanthal folds, arching eyebrows, thick everted lower lip, bilateral microtia with aural atresia, cleft palate, congenital tracheomalacia, brachidactyly, developmental delay.A female presented at birth with multiple congenital anomalies. Her mother had been taking 500 mg of mycophenolate mofetil (MM), twice a day and 40mg ofadalimumab every other week during the first 8 weeks of the pregnancy for lupus nephritis. No other medications were reported to have been taken. The child was born at 32 weeks' gestation by Caesarean section because of transverse position. The birth weight was 4422 g. Dysmorphic facial features noted at birth included arched eyebrows, hypertelorism, epicanthic folds, micrognathia and a thick everted lower lip. The child was also noted to have cleft palate, bilateral microtia with aural atresia (Figs 1 and 2) and brachy-dactyly.
机译:超视力,上epi褶,眉毛弓形,下唇浓密外翻,双侧小眼畸形伴有听觉闭锁,c裂,先天性气管软化,腕裂,发育迟缓。一例女性出生时有多种先天性异常。她的母亲在狼疮性肾炎的怀孕前八周每天服用500毫克霉酚酸酯(MM),每天两次,每隔一周服用40毫克阿达木单抗。据报道没有其他药物被服用。由于横卧,该孩子在剖腹产时妊娠32周时出生。出生体重为4422克。出生时发现的畸形面部特征包括眉毛拱形,过度精高,上皮褶皱,微棘皮症和下唇浓密的外翻。该儿童还被发现有pa裂,双侧小眼及耳闭锁(图1和2),且近距性。

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