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[双侧家族性无眼畸形]

[Bilateral familial anophthalmos].

作者信息

Manzini C, Orsini G B, Gualandri V

机构信息

Université de Milan, Faculté de Médecine et Chirurgie, Italie.

出版信息

J Fr Ophtalmol. 1988;11(8-9):593-4, 596.

PMID:3068284
Abstract

In the examined family the proband, a 14 months old male, presented a bilateral anophthalmos, bilateral cryptorchism, phimosis and decalcification of the nails. The palpebral fissures and the eyelids are smaller than normal; the orbit was empty, clad by a connective tissue without ocular buds. The testicles are unpalpable in the inguinal canal. The proband have a normal karyotype. Also a brother of the proband, dead for meningitis (age five months), had bilateral anophthalmos. The maternal branch of the family is lacking in hereditary pathology. On the contrary, the anamnesis of the paternal branch present very interesting data. His grandmother married twice; from the first marriage came, at the second generation, the sibship of the father, who had a sister with Franceschetti syndrome and another sister with double lower dental arch. From a second marriage originated, at the second generation, eleven siblings sibship, all seriously malformed and a dead infant, but the first-born having bilateral anophthalmos.

摘要

在所研究的这个家族中,先证者是一名14个月大的男性,患有双侧无眼畸形、双侧隐睾、包茎和指甲脱钙。睑裂和眼睑比正常情况小;眼眶为空,被没有眼芽的结缔组织覆盖。在腹股沟管内无法触及睾丸。先证者的核型正常。先证者的一个兄弟因脑膜炎死亡(5个月大),也患有双侧无眼畸形。家族的母系分支没有遗传病理学特征。相反,父系分支的病史呈现出非常有趣的数据。他的祖母结过两次婚;第一次婚姻的第二代是父亲的兄弟姐妹,其中一个姐妹患有弗朗西丝切蒂综合征,另一个姐妹有双侧下牙弓异常。第二次婚姻的第二代有11个兄弟姐妹,全都严重畸形,还有一个死婴,但其长子患有双侧无眼畸形。

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