Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.

D Bettio, D Giardino, N Rizzi, P Riva, L Volpi, E Barantani, A Tagliaferri, L Larizza
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引用次数: 9

Abstract

We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.

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垂体腺瘤Prader-Willi患者母体来源的同染色体15q。
我们报告了一个普雷德-威利综合征(PWS)患者携带平衡的15q15q易位,并受到泌乳素分泌垂体腺瘤的影响。分子研究表明,这种结构重排是母系同工染色体。根据同位体的鉴定作为罕见疾病关联的基础,以及最近关于垂体腺瘤中15号染色体单体和无体的报道,我们认为本例PWS可能与垂体腺瘤有关。
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