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新型早老样病症。

New progeroid disorder.

作者信息

Penttinen M, Niemi K M, Vinkka-Puhakka H, Johansson R, Aula P

机构信息

Clinical Genetics Unit, Turku University Central Hospital, Finland.

出版信息

Am J Med Genet. 1997 Mar 17;69(2):182-7.

PMID:9056558
Abstract

We report on a 10-year-old Caucasian male with a prematurely aged appearance, delayed bone maturation and dental development, pronounced acro-osteolysis with brachydactyly, and distinctive cutaneous findings including hard, confluent skin lesions with some clinical and histologic resemblance to those of juvenile hyaline fibromatosis (JHF). He also had hyperopia, sensorineural hearing loss, and elevated TSH. Linear growth and intellectual functions were normal. We believe that this patient represents a new progeroid disorder.

摘要

我们报告了一名10岁的白种男性,其外观过早衰老,骨骼成熟和牙齿发育延迟,伴有明显的肢端骨质溶解和短指畸形,以及独特的皮肤表现,包括坚硬、融合的皮肤病变,在临床和组织学上与青少年透明纤维瘤病(JHF)有些相似。他还患有远视、感音神经性听力损失和促甲状腺激素升高。线性生长和智力功能正常。我们认为该患者代表一种新的早老样疾病。

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