Le Caignec Cedric, Isidor Bertrand, de Pontbriand Ulrika, David Valerie, Audrezet Marie-Pierre, Ferec Claude, David Albert
Service de Génétique Médicale, Centre Hospitalo-Universitaire, Nantes, France.
Am J Med Genet A. 2007 Nov 15;143A(22):2696-9. doi: 10.1002/ajmg.a.31999.
Many patients with maternal uniparental disomy of chromosome 7 (UPD7) have been described, mainly with intrauterine and postnatal growth retardation or with Silver-Russell syndrome. In contrast, only three cases of paternal UPD7 have been reported, all associated with recessive disorders. Here, we report on the clinical and molecular data of the third patient with paternal UPD7 and cystic fibrosis. Pre- and postnatal growth were normal. These findings support the hypothesis that paternal isodisomy for human chromosome 7 may have no phenotypic effect on growth.
许多患有母源7号染色体单亲二倍体(UPD7)的患者已被描述,主要表现为宫内和出生后生长迟缓或患有Silver-Russell综合征。相比之下,仅报告了3例父源UPD7病例,均与隐性疾病相关。在此,我们报告了第三例患有父源UPD7和囊性纤维化患者的临床和分子数据。产前和产后生长均正常。这些发现支持了以下假设,即人类7号染色体的父源等二体可能对生长没有表型影响。