نتایج جستجو برای: anophthalmos

تعداد نتایج: 207  

Journal: :The journal of contemporary dental practice 2016
Sara Nader Marta Roberto Yoshio Kawakami Claudia Almeida Prado Piccino Sgavioli Ana Eliza Correa Guaniara D'Árk de Oliveira El Kadre Ricardo Sandri Carvalho

Waardenburg syndrome (WS) is an inherited autosomal dominant genetic disorder presenting variable penetrance and expressivity, with an estimated prevalence of 1:42,000. Clinical characteristics of WS include lateral displacement of the internal eye canthus, hyperplasia of the medial portion of the eyebrows, prominent and broad nasal base, congenital deafness, pigmentation of the iris and skin, ...

Journal: :Archives of pediatrics & adolescent medicine 2009
Krista S Crider Mario A Cleves Jennita Reefhuis Robert J Berry Charlotte A Hobbs Dale J Hu

OBJECTIVE To estimate the association between antibacterial medications and selected birth defects. DESIGN, SETTING, AND PARTICIPANTS Population-based, multisite, case-control study of women who had pregnancies affected by 1 of more than 30 eligible major birth defects identified via birth defect surveillance programs in 10 states (n = 13 155) and control women randomly selected from the same...

2013
Muhammad Khalil Ahmad Khan

Present study was conducted to evaluate the teratogenic effects of sublethal concentrations viz., 19.36, 9.7, and 4.8μg/g BW of deltamethrin, which was administered orally to the pregnant mice on day 6 of gestation. The fetuses were recovered on day 18 of gestation. The morphological studies revealed abnormalities including sacral hygromae, microcephally, micromelia, open eyelids, microphthalmi...

Journal: :Clinical genetics 2014
L Roos M Fang C Dali H Jensen N Christoffersen B Wu J Zhang R Xu P Harris X Xu K Grønskov Z Tümer

Anomalies of eye development can lead to the rare eye malformations microphthalmia and anophthalmia (small or absent ocular globes), which are genetically very heterogeneous. Several genes have been associated with microphthalmia and anophthalmia, and exome sequencing has contributed to the identification of new genes. Very recently, homozygous variations within ALDH1A3 have been associated wit...

Journal: :Journal of medical genetics 2014
Taraneh Esmailpour Hamidreza Riazifar Linan Liu Sandra Donkervoort Vincent H Huang Shreshtha Madaan Bassem M Shoucri Anke Busch Jie Wu Alexander Towbin Robert B Chadwick Adolfo Sequeira Marquis P Vawter Guoli Sun Jennifer J Johnston Leslie G Biesecker Riki Kawaguchi Hui Sun Virginia Kimonis Taosheng Huang

INTRODUCTION Lenz microphthalmia syndrome (LMS) is a genetically heterogeneous X-linked disorder characterised by microphthalmia/anophthalmia, skeletal abnormalities, genitourinary malformations, and anomalies of the digits, ears, and teeth. Intellectual disability and seizure disorders are seen in about 60% of affected males. To date, no gene has been identified for LMS in the microphthalmia s...

2005
Charles Shaw-Smith

Oesophageal atresia and/or tracheo-oesophageal fistula are common malformations occurring in approximately 1 in 3500 births. In around half of cases (syndromic oesophageal atresia), there are other associated anomalies, with cardiac malformations being the most common. These may occur as part of the VACTERL association (OMIM 192350). In the remainder of cases, oesophageal atresia/tracheo-oesoph...

Journal: :Molecular Vision 2008
Tristan White Tianyi Lu Ravikanth Metlapally James Katowitz Femida Kherani Tian-Yuan Wang Khanh-Nhat Tran-Viet Terri L. Young

PURPOSE Anophthalmia and microphthalmia (A/M) are rare congenital ocular malformations presenting with the absence of eye components or small eyes with or without structural abnormalities. A/M can be isolated or syndromic. The stimulated by retinoic acid gene 6 (STRA6) and Sloan-Kettering viral oncogene homolog (SKI) genes are involved in vitamin A metabolism, and are implicated with A/M develo...

Journal: :Birth defects research. Part B, Developmental and reproductive toxicology 2004
John M Rogers Kimberly C Brannen Brenda D Barbee Robert M Zucker Sigmund J Degitz

BACKGROUND Exposure of pregnant outbred CD-1 mice to methanol during the period of gastrulation results in exencephaly, cleft palate, and cervical vertebra malformations [Rogers and Mole, Teratology 55: 364, 1997], while inbred C57BL/6J mice are sensitive to the teratogenicity of ethanol. C57BL/6J fetuses exhibit the holoprosencephaly spectrum of malformations after maternal exposure to ethanol...

Journal: :Human molecular genetics 2006
Kathleen A Williamson Ann M Hever Joe Rainger R Curtis Rogers Alex Magee Zdenek Fiedler Wee Teik Keng Freddie H Sharkey Niolette McGill Clare J Hill Adele Schneider Mario Messina Peter D Turnpenny Judy A Fantes Veronica van Heyningen David R FitzPatrick

We report heterozygous, loss-of-function SOX2 mutations in three unrelated individuals with Anophthalmia-Esophageal-Genital (AEG) syndrome. One previously reported case [Rogers, R.C. (1988) Unknown cases. Proceedings of the Greenwood Genetic Center. 7, 57.] has a 2.7 Mb deletion encompassing SOX2 and associated with a cryptic translocation t(3;7)(q28;p21.3). The deletion and translocation break...

2008
JAMES CARROLL WOODARD PAUL M. NEWBERNE

Richardson & Hogan (1946) produced hydrocephalus in rats by feeding a purified casein diet containing all the vitamins available at that time. Almost 2 % of the young from females fed the experimental diet were hydrocephalic; female rats fed the same diet supplemented with liver extract gave birth to normal young. It is now thought that this diet was marginally deficient in vitamin B12 (Newbern...

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