Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑病是结肠的一种非炎症性、良性、可逆性的以色素沉着为特征的病
,该病的发生与长期便秘服用蒽琨
有关。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑病是结肠的一种非炎症性、良性、可逆性的以色素沉着为特征的病
,该病的发生与长期便秘服用蒽琨
有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑色素合成相关基
导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一
常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无明显自觉症状。
声明:以上例句、词性分均
互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一症性、良性、可逆性的以色素沉着为特征的病变,该病的发生与长期便秘服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的
。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
下、腹股沟、乳房下色素沉着15年,无明显自觉症状。
声明:以上例句、词性分类均互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一种非炎症性、良性、可逆性的以色素沉着为特征的病变,该病的发生与长期便秘琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
肤白化病是
于黑色素合成相关基因突变导
、
肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无明显自觉症状。
声明:以上例句、词性分类均互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一种非炎症性、良性、可逆性的沉着为特征的病变,该病的发生与长期便秘服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑
合成相关基因突变导致眼、皮肤、毛发黑
沉着减少或缺乏引起的一类
体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下沉着15年,无明显自觉症状。
声明:上例句、词性分类均
互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的种非炎症性、良性、可逆性的以色
为特征的病变,该病的发生与长期便秘服用蒽琨
泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑色
合成相关基因突变导致眼、皮肤、毛发黑色
减少或缺乏引起的
染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色15年,无明显自觉症状。
声明:以上例句、词性分均
互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一种非炎性、良性、可逆性的以色素沉着为特征的病变,该病的发生与长期便秘服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无明显状。
声明:以上例句、词性分类均互联网资源
动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一种非炎症性、良性、可逆性的色素沉着为特征的病变,该病的发生与长期便秘服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无显自觉症状。
:
上例句、词性分类均
互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠黑变病是结肠的一种非炎症性、良性、可逆性的以色素沉着为特征的病变,该病的生与长
服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮白化病是
于黑色素合成相关基因突变导致眼、皮
、
黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无明显自觉症状。
声明:以上例句、词性分类均互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若
现问题,欢迎向我们指正。
Conclusion Melanosis coli is inflammation,benign,reversibility chromatosis as characteristic,the disease is related to taking anthracene for long time constipation.
结论结肠变病是结肠的一种非炎症性、良性、可逆性的以色素沉着为特征的病变,该病的
生与
秘服用蒽琨类泻剂有关。
Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.
眼皮肤白化病是于
色素合成相关基因突变导致眼、皮肤、
色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。
Histopathology showed moderate hyperkeratosis and rete ridge elongation with the epidermal thinning above the papillar layer and a few melanophages in the dermis.
腋下、腹股沟、乳房下色素沉着15年,无明显自觉症状。
声明:以上例句、词性分类均互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若
现问题,欢迎向我们指正。