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携带致病基因女性中的X连锁智力障碍、性早熟伴肥胖症

X-linked intellectual handicap and precocious puberty with obesity in carrier females.

作者信息

Hockey A

出版信息

Am J Med Genet. 1986 Jan-Feb;23(1-2):127-37. doi: 10.1002/ajmg.1320230107.

DOI:10.1002/ajmg.1320230107
PMID:3953642
Abstract

Precocious puberty (PP) and intellectual handicap were present in 3 males in 2 generations of a Western Australian family. The 2 obligate carrier women were of normal intelligence but were grossly obese; one died of a cardiomyopathy at 55 years. The youngest affected male was found to have PP at 3 years. His mother was then pregnant, and because of her family history, was aware of the risk to have an affected male. Her mother had given birth to 2 sons with PP. By school age both of these males were mildly intellectually handicapped and this later became moderate. Apart from these 3 affected males, the 2 carriers lost 6 of their other 8 offspring, leaving only one normal woman and her unaffected son. The Fragile X test was negative on all males. This appears to be a new X-linked mental retardation syndrome, and a condition different from true idiopathic PP, or familial PP affecting both sexes, or PP with X-linked dominant inheritance.

摘要

在一个西澳大利亚家庭的两代人中,有3名男性出现性早熟(PP)和智力障碍。2名必然携带者女性智力正常,但严重肥胖;其中一名在55岁时死于心肌病。最年轻的患病男性在3岁时被发现患有性早熟。当时他的母亲怀孕了,由于家族病史,她意识到生下患病男性的风险。她的母亲曾生下2名患有性早熟的儿子。到学龄期,这两名男性均有轻度智力障碍,后来发展为中度。除了这3名患病男性外,2名携带者的其他8个后代中有6个夭折,仅剩下一名正常女性及其未患病的儿子。所有男性的脆性X检测均为阴性。这似乎是一种新的X连锁智力障碍综合征,与真正的特发性性早熟、或影响两性的家族性性早熟、或具有X连锁显性遗传的性早熟不同。

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