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先天性青光眼、肢体畸形、骨骼发育不良及面部异常:另一家族报告

Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.

作者信息

Mégarbané A, Tomey K, Wakim G

机构信息

Laboratoires de Biologie Moléculaire et Cytogénétique, Faculté de Médecine, Université Saint Joseph, Paris, France.

出版信息

Am J Med Genet. 1997 Nov 28;73(1):67-71. doi: 10.1002/(sici)1096-8628(19971128)73:1<67::aid-ajmg13>3.0.co;2-p.

Abstract

We report on a family of first cousin parents in which 2 of 3 children presented with congenital glaucoma, large anterior fontanelle, prominent forehead, hypertelorism, down-slanting palpebral fissures, broad and flat nasal bridge, broad nasal tip, anteverted nostrils, high-arched palate, gingival hypertrophy, pectus excavatum, prominent coccyx with skin fold, short fingers and toes, single palmar creases, flexion deformities of fingers, club feet, and osseous malformations. Despite some clinical differences, their anomalies are very similar to those seen in a new and rare autosomal recessive entity described by ter Haar et al. [1982]. Differential diagnoses are discussed.

摘要

我们报告了一对表亲父母的家庭,他们的3个孩子中有2个患有先天性青光眼、前囟门大、额头突出、眼距过宽、睑裂向下倾斜、鼻梁宽而扁平、鼻尖宽阔、鼻孔前倾、高拱腭、牙龈肥大、漏斗胸、尾骨突出伴皮肤褶皱、手指和脚趾短小、单一掌纹、手指屈曲畸形、马蹄内翻足以及骨骼畸形。尽管存在一些临床差异,但他们的异常情况与ter Haar等人[1982年]描述的一种新的罕见常染色体隐性疾病所见的异常非常相似。文中讨论了鉴别诊断。

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