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A Case of Bloom Syndrome With Uncommon Clinical Manifestations Confirmed on Genetic Testing

机译:基因检测证实布鲁姆综合症临床表现罕见

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Bloom syndrome, a rare autosomal-recessive disorder, characteristically presents with photosensitivity, telangiectatic facial erythema, and growth deficiency. We present a case of Bloom syndrome with uncommon clinical manifestations including alopecia areata, eyebrow hair loss, flat nose, reticular pigmentation, and short sharpened distal phalanges with fingernails that were wider than they were long. We detected the Bloom syndrome gene, BLM, which is one of the members of the RecQ family of DNA helicases, and found changes in 2 heterozygous nucleotide sites in the patient as well as her father and mother.
机译:布鲁姆综合征是一种罕见的常染色体隐性遗传疾病,典型表现为光敏性,毛细血管扩张性面部红斑和生长不足。我们介绍了一例布鲁姆综合征,其临床表现不常见,包括斑秃,眉毛脱发,鼻子平直,网状色素沉着以及末端尖锐的短指骨,指甲长于其长。我们检测到了布鲁姆综合症基因BLM,它是DNA解旋酶RecQ家族的成员之一,并发现患者及其父亲和母亲的2个杂合核苷酸位点发生了变化。

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