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齐默尔曼-拉班德综合征:进一步的临床描述。

Zimmermann-Laband syndrome: further clinical delineation.

作者信息

Dávalos I P, García-Cruz D, García-Cruz M O, Ramírez-Dueñas M L, Solis-Cámara P, Correa-Cerro L S, Perez-Rulfo D, Sánchez-Corona J

机构信息

Divisiones de Genética, CIBO, CMNO, IMSS, Guadalajara, Jalisco, Mexico.

出版信息

Genet Couns. 2005;16(3):283-90.

Abstract

Zimmermann-Laband syndrome (ZLS) is an autosomal dominant disorder characterized by gingival fibromatosis, absent or dysplastic distal phalanges, vertebral defects, hepatosplenomegaly, hypertrichosis and sometimes mental retardation. We describe two unrelated patients, a girl aged 9 years and a boy 11 months whose clinical and radiological findings permit us to diagnose the ZLS. Body overgrowth, present in both patients, was identified as a main clinical feature not previously reported as well as the presence in neuroimaging studies of a cavernous hemangioma on the frontal and the left cerebellar regions in the boy. The girl also presented important radiological characteristics such as broad medulary canals and metaphyses of long bones, thin cortices, broad ribs, accelerated skeletal maturation as well as high intelligence level. A wide clinical spectrum in ZLS is also considered.

摘要

齐默尔曼 - 拉班德综合征(ZLS)是一种常染色体显性疾病,其特征为牙龈纤维瘤病、远端指骨缺失或发育异常、脊椎缺陷、肝脾肿大、多毛症,有时还伴有智力发育迟缓。我们描述了两名无血缘关系的患者,一名9岁女孩和一名11个月大的男孩,他们的临床和影像学检查结果使我们得以诊断出ZLS。两名患者均出现身体过度生长,这被确定为一个此前未报告过的主要临床特征,此外,在男孩的神经影像学研究中还发现其额叶和左小脑区域存在海绵状血管瘤。该女孩还呈现出重要的放射学特征,如长骨髓腔和干骺端增宽、皮质变薄、肋骨增宽、骨骼成熟加速以及智力水平较高。本文还探讨了ZLS广泛的临床谱。

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