遗传疾病

At present, the foreign reports show that Freck1e is the followed trait of some diseases such as xeroderma pigmeniosa, incontineniia pigmenti and PJS syndrome.

目前，国外对本病的相关报道均认为该病为其它疾病的伴随性状如着色性干皮病、色素失禁症、PJS综合症等，其遗传方式不明。

Alstrom syndrome is a rare autosomal recessive disorder associated with early childhood retinopathy, progressive sensorineural hearing loss, truncal obesity, and acanthosis nigricans.

Alstrom症是一种自体陷性遗传的疾病，伴随有幼年型视网膜病变，进行性神经听力丧失，躯干肥胖及黑色棘皮症。

These disorders, with one exception, are inherited as autosomal recessive traits.

这些疾病中，有一个例外，是为常染色体隐性遗传特徵。

By report, DPR female in this general disease reason clan hands down to younger generation by heredity , show the various different symptom generally besides the patient perspires except not having a fingerprint and not having no way,for example hair cutting off , having on skin chromatosis and so on easy to sparse , not to have the tooth , nail cachexic.

据悉，DPR这种疾病通常由家族中的女性遗传给下一代，患者除了没有指纹和无法排汗之外，通常还表现出多种不同症状，例如头发稀疏、没有牙齿、指甲营养不良易断、皮肤上有色素沉着等等。

By report, DPR female in this general disease reason clan hands down to younger generation by heredity , show the various different symptom generally besides the patient perspires except not having a fingerprint and not having no way,for example hair cutting off , having on skin chromatosis and so on easy to sparse , not to have the tooth , nail cachexic.

本新闻共4页，当前在第2页 1 2 3 4据悉，DPR这种疾病通常由家族中的女性遗传给下一代，患者除了没有指纹和无法排汗之外，通常还表现出多种不同症状，例如头发稀疏、没有牙齿、指甲营养不良易断、皮肤上有色素沉着等等。

P6 _ R By report, DPR female in this general disease reason clan hands down to younger generation by heredity , show the various different symptom generally besides the patient perspires except not having a fingerprint and not having no way,for example hair cutting off , having on skin chromatosis and so on easy to sparse , not to have the tooth , nail cachexic.

据悉，DPR这种疾病通常由家族中的女性遗传给下一代，患者除了没有指纹和无法排汗之外，通常还表现出多种不同症状，例如头发稀疏、没有牙齿、指甲营养不良易断、皮肤上有色素沉着等等。

M0 P By report, DPR female in this general disease reason clan hands down to younger generation by heredity , show the various different symptom generally besides the patient perspires except not having a fingerprint and not having no way,for example hair cutting off , having on skin chromatosis and so on easy to sparse , not to have the tooth , nail cachexic.

据悉，DPR这种疾病通常由家族中的女性遗传给下一代，患者除了没有指纹和无法排汗之外，通常还表现出多种不同症状，例如头发稀疏、没有牙齿、指甲营养不良易断、皮肤上有色素沉着等等。

In humans, genetic defects of CathA cause galactosialidosis, a metabolic disease characterized by combined deficiency of CathA, GAL, and Neu1 and a lysosomal storage of sialylated glycoconjugates.

在人类，CathA的遗传缺失可引起半乳糖唾液酸沉积症，一种以CathA、 GAL、 Neu1不足和唾液酸化糖结合物在溶酶体的沉为特征的代谢疾病。

Cleidocranial dysplasia is a rare syndrome usually caused by an autosomal dominant gene without gender predilection.

颅锁骨发育不全是一种罕见体染色体显性遗传的疾病，男女发生的比率相当。

Genetic defects in telomere maintenance result in dyskeratosis congenita, a family of diseases characterised by deterioration of rapidly-renewing tissues.

端粒维持的遗传缺陷导致角质化不良症（ dyskeratosis congenita ， DC ），这是一组疾病，特征是迅速更新组织的退行性变化。

Since historical times,England ,where the early inhabitants were Celts, has been conquered three times .

从有历史以来，英国，在此地早期居住的是凯尔特人，已经被征服了三次。

Bluetooth OBEX File Transfer Enables the sending and receiving of files on your phone via Bluetooth.

蓝牙OBEX文件移动允许经过蓝牙传送和接受文件。。。。