Literature DB >> 10340646

Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.

J Slee1, G Lam, I Walpole.   

Abstract

We present two sisters with microcephaly, developmental delay, marked microphthalmia, congenital cataracts, cerebral and cerebellar hypoplasia, and intracranial calcification. No evidence of intrauterine infection was found. There have been previous reports of microcephaly, intracranial calcification, and an intrauterine infection-like autosomal recessive condition, but the sibs in this report appear to represent a more severe form of such a condition or a previously undescribed entity.

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Year:  1999        PMID: 10340646

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation.

Authors:  Manèl Chograni; Myriam Chaabouni; Imen Chelly; Mohamed Bechir Helayem; Habiba Chaabouni-Bouhamed
Journal:  Mol Vis       Date:  2010-04-03       Impact factor: 2.367

2.  A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset.

Authors:  Domenico Umberto De Rose; Francesca Gallini; Domenica Immacolata Battaglia; Eloisa Tiberi; Simona Gaudino; Ilaria Contaldo; Chiara Veredice; Domenico Marco Romeo; Luca Massimi; Alessia Asaro; Cristina Cereda; Giovanni Vento; Eugenio Maria Mercuri
Journal:  Neurol Sci       Date:  2021-07-22       Impact factor: 3.307

Review 3.  Immunogenetics of the Ocular Anterior Segment: Lessons from Inherited Disorders.

Authors:  Jasmine Y Serpen; Stephen T Armenti; Lev Prasov
Journal:  J Ophthalmol       Date:  2021-06-28       Impact factor: 1.909

  3 in total

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