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Hutchinson-Gilford progeria syndrome in a 45-year-old man.

作者信息

Ogihara T, Hata T, Tanaka K, Fukuchi K, Tabuchi Y, Kumahara Y

出版信息

Am J Med. 1986 Jul;81(1):135-8. doi: 10.1016/0002-9343(86)90196-8.

DOI:10.1016/0002-9343(86)90196-8
PMID:3728539
Abstract

A 45-year-old man with typical Hutchinson-Gilford progeria syndrome is described. The patient had the characteristic physical findings of this syndrome, such as short stature, "horse-riding" stance, coxa valga, alopecia, micrognathia, craniofacial disproportion, and prominent eyes. He had refractory congestive heart failure due to arteriosclerotic heart disease and hypertension, and he also had arteriosclerosis obliterans. Some immunologic and endocrinologic abnormalities commonly seen in the elderly were present in this patient. On the basis of a review of the literature, this is the first patient with this syndrome who had survived into the fourth decade.

摘要

相似文献

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Am J Med. 1986 Jul;81(1):135-8. doi: 10.1016/0002-9343(86)90196-8.
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引用本文的文献

1
Hutchinson-Gilford progeria syndrome in siblings. Report of three new cases.
Skeletal Radiol. 1990;19(8):585-90. doi: 10.1007/BF00241281.