英语翻译NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues.It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF),including café-au-lait spots,a

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英语翻译NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues.It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF),including café-au-lait spots,a

英语翻译NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues.It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF),including café-au-lait spots,a
英语翻译
NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues.It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF),including café-au-lait spots,axillary freckles and hyperpigmentation overlying plexiform neurofibromas.In addition,associations of NF with naevus spilus,naevus of Ota,segmental unilateral melanosis and congenital giant melanocytic naevus have been anecdotally described.We present a rare case of hyperpigmentation overlying plexiform neurofibroma in the waist and buttock of a woman with NF1.

英语翻译NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues.It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF),including café-au-lait spots,a
NF1 öncelikle sinir hücresi dokuların gelişimi ve büyüme etkileyen otozomal dominant bir hastalıktır.Bu pigmente deri lezyonlarının çeşitli pleksiform nörofibroma örten café-au-lait lekeleri,aksiller çiller ve hiperpigmentasyon gibi nörofibromatozis (NF) ile ilişkili olduğu bilinmektedir.Buna ek olarak,nevus Spilus,Ota nevus,segmental tek taraflı melanoz ve konjenital dev melanositik ile NF birlikleri kısa olarak tarif edilmiştir.Biz NF1 ile bir kadının bel ve kalça bölgesindeki hiperpigmentasyon üstteki pleksiform nörofibroma nadir bir olgu sunuldu.

基因是一种常染色体显性遗传疾病,主要影响发展和神经细胞组织生长。众所周知,各类色素性皮肤病变与神经纤维瘤病(因子),包括咖啡é- au-lait斑点,雀斑,色素沉着覆腋丛状神经纤维瘤。此外,协会的因子与痣痣,太田痣,节段性单侧黑变病和先天性巨黑色素细胞痣已升温的描述。我们提出一例罕见的色素沉着覆丛状神经纤维瘤在腰和臀部的女人NF....

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基因是一种常染色体显性遗传疾病,主要影响发展和神经细胞组织生长。众所周知,各类色素性皮肤病变与神经纤维瘤病(因子),包括咖啡é- au-lait斑点,雀斑,色素沉着覆腋丛状神经纤维瘤。此外,协会的因子与痣痣,太田痣,节段性单侧黑变病和先天性巨黑色素细胞痣已升温的描述。我们提出一例罕见的色素沉着覆丛状神经纤维瘤在腰和臀部的女人NF.

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NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues. It is known that various kinds of pigmented skin lesions are associated with neurofibromatos...

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NF1 is an autosomal dominant disorder primarily affecting the development and growth of nerve cell tissues. It is known that various kinds of pigmented skin lesions are associated with neurofibromatosis (NF), including café-au-lait spots, axillary freckles and hyperpigmentation overlying plexiform neurofibromas. In addition, associations of NF with naevus spilus, naevus of Ota, segmental unilateral melanosis and congenital giant melanocytic naevus have been anecdotally described. We present a rare case of hyperpigmentation overlying plexiform neurofibroma in the waist and buttock of a woman with NF1.

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