Höglund P, Holmberg C, de la Chapelle A, Kere J
Department of Medical Genetics, University of Helsinki, Finland.
Am J Hum Genet. 1994 Oct;55(4):747-52.
Uniparental disomy for maternal chromosome 7 has been described in three patients with recessive disorders. Short stature in each of these patients has been explained by the effect of imprinting of growth-related genes on maternal chromosome 7. Alternatively, although less likely, all these patients may be homozygous for a rare recessive mutation. Here we report both paternal isodisomy for chromosome 7 and normal growth in a patient with a recessive disorder, congenital chloride diarrhea. She had inherited only paternal alleles at 10 loci and was homozygous for another 10 chromosome 7 loci studied. Her physical status and laboratory tests were normal except for a mild high-frequency sensorineural hearing loss. As the patient has normal stature, it is likely that the paternal chromosome 7 lacks the suggested maternal imprinting effect on growth. Paternal isodisomy for human chromosome 7 may have no phenotypic effect on growth.
三名患有隐性疾病的患者被发现存在母源7号染色体单亲二体现象。这些患者身材矮小均被解释为母源7号染色体上与生长相关基因的印记效应所致。另外,尽管可能性较小,但所有这些患者可能都是一种罕见隐性突变的纯合子。在此,我们报告了一名患有隐性疾病——先天性氯腹泻的患者,其存在父源7号染色体等臂二体且生长正常。她在10个位点仅遗传了父源等位基因,在所研究的另外10个7号染色体位点上为纯合子。除轻度高频感音神经性听力损失外,她的身体状况和实验室检查均正常。由于该患者身材正常,父源7号染色体可能不存在对生长的母源印记效应。人类7号染色体的父源等臂二体可能对生长没有表型影响。