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关注：1
2013-05-23 12:21
求翻译：Congenital causes of hypogonadotropic hypoonadisminclude Kallmann syndrome, which is mostcommonly due to a mutation in the KAL1 gene and is characterized by anosmia, cleft palate, cryptorchidism,and congenital failure of hypothalamic gonadotropinreleasing hormone (GnRH) secretion.是什么意思？ 待解决
 悬赏分：1
- 离问题结束还有
Congenital causes of hypogonadotropic hypoonadisminclude Kallmann syndrome, which is mostcommonly due to a mutation in the KAL1 gene and is characterized by anosmia, cleft palate, cryptorchidism,and congenital failure of hypothalamic gonadotropinreleasing hormone (GnRH) secretion.
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2013-05-23 12:21:38
hypogonadotropic hypoonadisminclude Kallmann综合征mostcommonly，这是由于在KAL1基因突变的特点是嗅觉丧失，腭裂，隐睾，先天性故障，下丘脑gonadotropinreleasing激素（GnRH）的分泌的先天性原因。
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2013-05-23 12:23:18
这一特点是长期的先天原因hypoonadisminclude卡尔曼综合症,这是由于一个mostcommonly突变基因的1大韩航空和的特点是anosmia、裂颚,cryptorchidism」的失败和先天性hypothalamic gonadotropinreleasing激素(gnrh)分泌。
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2013-05-23 12:24:58
hypogonadotropic hypoonadisminclude Kallmann综合症状的先天起因， mostcommonly归结于一个变化在KAL1基因和描绘为嗅觉缺失、豁嘴、隐睾病和下丘脑gonadotropinreleasing的激素(GnRH)分泌物的先天失败。
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2013-05-23 12:26:38
先天性的青少年 hypoonadisminclude 功能低下综合症，这是由于到 KAL1 基因突变，特点是嗅觉障碍、 腭裂、 隐睾症、 和下丘脑 gonadotropinreleasing (GnRH) 激素分泌的先天性失败的原因。
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2013-05-23 12:28:18
先天性的青少年 hypoonadisminclude 功能低下综合症，这是由于到 KAL1 基因突变，特点是嗅觉障碍、 腭裂、 隐睾症、 和下丘脑 gonadotropinreleasing (GnRH) 激素分泌的先天性失败的原因。
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