Kassner E G, Haller J O, Reddy V H, Mitarotundo A, Katz I
AJR Am J Roentgenol. 1976 Dec;127(6):927-33. doi: 10.2214/ajr.127.6.927.
Frontometaphyseal dysplasia is a syndrome that encompasses cranial hyperostosis, abnormal tubulation of cylindrical bones, and other skeletal and extraskeletal abnormalities. The most striking features are overgrowth of the supraorbital ridges which results in a Mephistophelian facial appearance and a radiographic configuration of the skull that has been likened to a soldier's helmet. Most patients have severe hearing loss, defective dentition, poorly developed musculature, and joint contractures. Dominant inheritance has been suggested in previous reports, but an appropriate pedigree has been documented in only one family. This paper describes three additional patients in two unrelated families: (1) an 8-year-old boy whose mother has mild metaphyseal dysplasia and several minor skeletal abnormalities that have occurred in patients with the syndrome; and (2) two maternal half-brothers. These cases provide additional evidence that frontometaphyseal dysplasia is an autosomal dominant trait with variable penetrance.
额骨干骺端发育异常是一种综合征,包括颅骨骨质增生、长管状骨管状结构异常以及其他骨骼和骨骼外异常。最显著的特征是眶上嵴过度生长,导致面部呈现出梅菲斯特般的外观,以及颅骨的影像学表现类似于士兵的头盔。大多数患者有严重听力损失、牙列缺陷、肌肉发育不良和关节挛缩。先前的报告提示为显性遗传,但仅有一个家族记录了合适的家系。本文描述了两个无关家族中的另外三名患者:(1)一名8岁男孩,其母亲有轻度干骺端发育异常以及该综合征患者中出现的一些轻微骨骼异常;(2)两名同父异母的兄弟。这些病例提供了额外的证据,证明额骨干骺端发育异常是一种具有可变外显率的常染色体显性性状。