نتایج جستجو برای: anophthalmos

تعداد نتایج: 207  

Journal: :The Journal of clinical endocrinology and metabolism 2008
Daniel Kelberman Sandra C P de Castro Shuwen Huang John A Crolla Rodger Palmer John W Gregory David Taylor Luciano Cavallo Maria F Faienza Rita Fischetto John C Achermann Juan Pedro Martinez-Barbera Karine Rizzoti Robin Lovell-Badge Iain C A F Robinson Dianne Gerrelli Mehul T Dattani

CONTEXT Heterozygous, de novo mutations in the transcription factor SOX2 are associated with bilateral anophthalmia or severe microphthalmia and hypopituitarism. Variable additional abnormalities include defects of the corpus callosum and hippocampus. OBJECTIVE We have ascertained a further three patients with severe eye defects and pituitary abnormalities who were screened for mutations in S...

2015
Beatriz López-Escobar David A. Cano Anabel Rojas Beatriz de Felipe Francisco Palma José A. Sánchez-Alcázar Deborah Henderson Patricia Ybot-González

Embryopathies that develop as a consequence of maternal diabetes have been studied intensely in both experimental and clinical scenarios. Accordingly, hyperglycaemia has been shown to downregulate the expression of elements in the non-canonical Wnt-PCP pathway, such as the Dishevelled-associated activator of morphogenesis 1 (Daam1) and Vangl2. Daam1 is a formin that is essential for actin polym...

Journal: :Genesis 2001
P Tucker L Laemle A Munson S Kanekar E R Oliver N Brown H Schlecht M Vetter T Glaser

The eyeless inbred mouse strain ZRDCT has long served as a spontaneous model for human anophthalmia and the evolutionary reduction of eyes that has occurred in some naturally blind mammals. ZRDCT mice have orbits but lack eyes and optic tracts and have hypothalamic abnormalities. Segregation data suggest that a small number of interacting genes are responsible, including at least one major rece...

Journal: :Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus 2003
Medhat F Guirgis Agnes M F Wong Lawrence Tychsen

C audal regression syndrome (CRS) is a rare embryopathy characterized by maldevelopment of the vertebrae, visceral organs, and lower extremities. Patients with CRS have deformities of the sacrococcygeal vertebrae and develop neurogenic bladder from dysfunction of the sacral nerve root. Additional anomalies include congenital heart defects, intestinal malrotation, agenesis of the genitourinary s...

Journal: :Mechanisms of Development 2009
Hideyo Ohuchi Hitomi Fukui Akane Matsuyo Sayuri Tomonari Sumihare Noji

Orbital cartilage encircles the eye giving strength and support to the neural retina. It is derived from cranial neural crest cells (NCCs), cells that can generate a number of cell types including neurons, glia, and melanocytes. Uniquely in the head, NCCs also make skeletal derivatives that form the majority of the craniofacial skeleton. Differentiation of NCCs into cartilage requires inductive...

Journal: :The Journal of Experimental Medicine 1982
C C Leung

A glycoprotein with an apparent 340,000 mol wt (gp 340K) was isolated from rat kidney saline-soluble extract by ammonium sulfate precipitation, DE 52 ion-exchange cellulose chromatography, concanavalin A affinity column, Sephacryl S-300 gel filtration, and discontinuous polyacrylamide gel electrophoresis (PAGE). The relative purity of gp 340K was examined by double immunodiffusion analysis, dis...

2011
Joe Rainger Ellen van Beusekom Jacqueline K. Ramsay Lisa McKie Lihadh Al-Gazali Rosanna Pallotta Anita Saponari Peter Branney Malcolm Fisher Harris Morrison Louise Bicknell Philippe Gautier Paul Perry Kishan Sokhi David Sexton Tanya M. Bardakjian Adele S. Schneider Nursel Elcioglu Ferda Ozkinay Rainer Koenig Andre Mégarbané C. Nur Semerci Ayesha Khan Saemah Zafar Raoul Hennekam Sérgio B. Sousa Lina Ramos Livia Garavelli Andrea Superti Furga Anita Wischmeijer Ian J. Jackson Gabriele Gillessen-Kaesbach Han G. Brunner Dagmar Wieczorek Hans van Bokhoven David R. FitzPatrick

Ophthalmo-acromelic syndrome (OAS), also known as Waardenburg Anophthalmia syndrome, is defined by the combination of eye malformations, most commonly bilateral anophthalmia, with post-axial oligosyndactyly. Homozygosity mapping and subsequent targeted mutation analysis of a locus on 14q24.2 identified homozygous mutations in SMOC1 (SPARC-related modular calcium binding 1) in eight unrelated fa...

Journal: :Human molecular genetics 2013
Mani Yahyavi Hana Abouzeid Ghada Gawdat Anne-Sophie de Preux Tong Xiao Tanya Bardakjian Adele Schneider Alex Choi Eric Jorgenson Herwig Baier Mohamad El Sada Daniel F Schorderet Anne M Slavotinek

The major active retinoid, all-trans retinoic acid, has long been recognized as critical for the development of several organs, including the eye. Mutations in STRA6, the gene encoding the cellular receptor for vitamin A, in patients with Matthew-Wood syndrome and anophthalmia/microphthalmia (A/M), have previously demonstrated the importance of retinol metabolism in human eye disease. We used h...

Journal: :Ceska gynekologie 2006
A Sípek V Gregor J Horácek D Masátová

OBJECTIVE An analysis of birth defects incidence in offspring of mothers taking 1st trimester medication in the Czech Republic in 1996-2004. TYPE OF STUDY A retrospective demographical-epidemiological analysis of data from a National Register of Congenital Anomalies of the Czech Republic. METHODOLOGY Data on birth defects in the Czech Republic from the Institute of Health Information and St...

Journal: :American journal of human genetics 2014
Joe Rainger Davut Pehlivan Stefan Johansson Hemant Bengani Luis Sanchez-Pulido Kathleen A Williamson Mehmet Ture Heather Barker Karen Rosendahl Jürgen Spranger Denise Horn Alison Meynert James A B Floyd Trine Prescott Carl A Anderson Jacqueline K Rainger Ender Karaca Claudia Gonzaga-Jauregui Shalini Jhangiani Donna M Muzny Anne Seawright Dinesh C Soares Mira Kharbanda Victoria Murday Andrew Finch Richard A Gibbs Veronica van Heyningen Martin S Taylor Tahsin Yakut Per M Knappskog Matthew E Hurles Chris P Ponting James R Lupski Gunnar Houge David R FitzPatrick

We identified four different missense mutations in the single-exon gene MAB21L2 in eight individuals with bilateral eye malformations from five unrelated families via three independent exome sequencing projects. Three mutational events altered the same amino acid (Arg51), and two were identical de novo mutations (c.151C>T [p.Arg51Cys]) in unrelated children with bilateral anophthalmia, intellec...

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