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眼下颌面骨发育不全(哈勒曼-施特雷夫综合征)中的牙槽骨异常。

Dento-alveolar abnormalities in oculomandibulodyscephaly (Hallermann-Streiff syndrome).

作者信息

Slootweg P J, Huber J

出版信息

J Oral Pathol. 1984 Apr;13(2):147-54. doi: 10.1111/j.1600-0714.1984.tb01411.x.

DOI:10.1111/j.1600-0714.1984.tb01411.x
PMID:6425475
Abstract

Oculomandibulodyscephaly (OMD) is characterized by anomalies of skull, mandible, skin and eyes and also by a proportionate nanism. Dental abnormalities are often observed but poorly defined. Examination of a 2-month-old infant that suffered from OMD, having died from an unrelated cause revealed premature eruption of several deciduous teeth, crowding of unerupted deciduous teeth and agenesis of all permanent teeth excepting the first permanent molars.

摘要

眼下颌面骨发育不全(OMD)的特征是颅骨、下颌骨、皮肤和眼睛出现异常,以及身材比例矮小。常观察到牙齿异常,但描述不明确。对一名患有OMD的2个月大婴儿进行检查,该婴儿死于无关病因,结果显示几颗乳牙过早萌出、未萌出乳牙拥挤以及除第一恒磨牙外所有恒牙先天性缺失。

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Dento-alveolar abnormalities in oculomandibulodyscephaly (Hallermann-Streiff syndrome).眼下颌面骨发育不全(哈勒曼-施特雷夫综合征)中的牙槽骨异常。
J Oral Pathol. 1984 Apr;13(2):147-54. doi: 10.1111/j.1600-0714.1984.tb01411.x.
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[Hallermann-Streiff-Francois- syndrome. (Oculo-mandibulo-dyscrania with hypotrichosis). A most characteristic syndrome with dyscrania and hypotrichosis, facial and eye anomalies and dwarfism].
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Hallermann-Streiff syndrome.哈勒曼-施特雷夫综合征。
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