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*  Aniridia
PMID 19390808 Aniridia Foundation International - AFI Aniridia Europe GeneReviews/NCBI/NIH/UW entry on Aniridia OMIM entries on ... Sporadic aniridia mutations may affect the WT1 region adjacent to the AN2 aniridia region, causing a kidney cancer called ... Aniridia may be broadly divided into hereditary and sporadic forms. Hereditary aniridia is usually transmitted in an autosomal ... Defects in the PAX6 gene cause aniridia-like ocular defects in mice (as well as Drosophila). Aniridia is a heterozygous ...
*  Aniridia renal agenesis psychomotor retardation
Aniridia ataxia renal agenesis psychomotor retardation is a rare genetic disorder characterized by missing irises of the eye, ... "Aniridia renal agenesis psychomotor retardation , Genetic and Rare Diseases Information Center (GARD) - an NCATS Program". ... http://www.wrongdiagnosis.com/a/aniridia_ataxia_renal_agenesis_psychomotor_retardation/intro.htm "Aniridia renal agenesis ...
*  DMOZ - Health: Conditions and Diseases: Eye Disorders: Aniridia
Aniridia is an eye condition that effects the development of the eye in children. Typically it stops the eye developing before ... Aniridia is an eye condition that effects the development of the eye in children. Typically it stops the eye developing before ...
*  List of OMIM disorder codes
COL4A1 Aniridia; 106210; PAX6 Anonychia congenita; 206800; RSPO4 Anterior segment mesenchymal dysgenesis; 107250; FOXE3 ...
*  WAGR syndrome
... (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic ... While aniridia is rarely absent in WAGR syndrome, cases have been reported without it. Chromosomal analysis is necessary for ... Newborn children with WAGR syndrome are soon noted to have aniridia. The clinical suspicion for WAGR may be increased with the ... In older children, clinical diagnosis of the syndrome can be made when aniridia and one of the other features are present. ...
*  Macular hypoplasia
Aniridia Network - Fovea/Macula Hypoplasia. ...
*  Anil Kumar Mandal
CS1 maint: Multiple names: authors list (link) Aniridia Trabeculectomy Buphthalmos Aphakia India portal Medicine portal Long ... "Clinical Manifestations of Congenital Aniridia". Journal of Pediatric Ophthalmology & Strabismus. 51 (1): 5962. doi:10.3928/ ...
*  PAX6
1994). "Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins". Am. J. Hum. Genet. 54 (5 ... Microphthalmia Overview GeneReviews/NCBI/NIH/UW entry on Aniridia OMIM entries on Aniridia Gene Expression Patterns from the ... Paired box protein Pax-6, also known as aniridia type II protein (AN2) or oculorhombin, is a protein that in humans is encoded ... Hanson I, Brown A, van Heyningen V (1995). "A new PAX6 mutation in familial aniridia". J. Med. Genet. 32 (6): 488-9. doi: ...
*  Heterochromia iridum
"Bilateral Duane syndrome and bilateral aniridia". J AAPOS. 10 (3): 273-4. doi:10.1016/j.jaapos.2006.02.002. PMID 16814183. ...
*  Hemeralopia
Adie's pupil which fails to constrict in response to light; Aniridia, which is absence of the iris; Albinism where the iris is ...
*  Gillespie syndrome
Early onset partial aniridia, cerebellar ataxia, and mental retardation are hallmark of syndrome. The iris abnormality is ... The aniridia consisting of a superior coloboma and inferior iris hypoplasia, foveomacular dysplasia. Atypical Gillespie ... The disorder is characterized by partial aniridia (meaning that part of the iris is missing), ataxia (motor and coordination ... PAX6 gene analysis can also be helpful to distinguish between autosomal dominant aniridia and Gillespie syndrome. However ...
*  Glued IOL
The glued IOL technique can be used in cases in which there is aphakia with aniridia (Fig 7 A and B). In such a cases one can ... Thus we can get an aniridia glued IOL. This procedure combines two techniques i.e. Glued IOL and IOL Scaffold. In this ... aniridia with cataractous subluxated lens, Weill-Marchesani syndrome with microspherophakia and glaucoma. In dislocated ... use an aniridia IOL which has got an artificial iris with the IOL component. ...
*  Santosh G. Honavar
Frosted Iris Intraocular Lens in Traumatic Aniridia with Cataract. Ophthalmic Surgery 1994; 25: 730-734. 238. Vajpayee RB, ...
*  VTPP 652 Pax-6
... deletion results in aniridia, autism and mental retardation". Human Genetics. 123 (4): 371-378. doi:10.1007/s00439-008-0484-x. ...
*  Boston keratoprosthesis
The Boston KPro is a proven primary treatment option for repeat graft failure, herpetic keratitis, aniridia and many pediatric ... Outcomes of Boston keratoprosthesis in aniridia: a retrospective multicenter study. Am J Ophthalmol. Aug 2007;144(2):227-231 ...
*  Corneal neovascularization
CNV causes may be congenital in nature, such as with Aniridia, or acquired. Frequently, inflammatory, infectious, degenerative ...
*  Zamzam-Sheriff-Phillips syndrome
It is characterized by aniridia, ectopia lentis, abnormal upper incisors and intellectual disability. Not a lot of research has ... Zazam Sheriff Phillips syndrome; Aniridia, lens luxation, mental retardation at NIH's Office of Rare Diseases Birth Disorder ... Information Directory - Z Zamzam AM, Sheriff SM, Phillips CI (1988). "Aniridia, ectopia lentis, abnormal upper incisors and ...
*  Lazier Partners Racing
Support for the institute was given as Buddy Lazier's daughter Jacqueline suffers from Aniridia. Team support is being provided ...
*  Pannus
... may also develop in diseases of the corneal stem cells, such as aniridia. It is often resolved by peritomy. Farlex ...
*  Eye color
ISBN 1-139-44931-1. Aniridia at eMedicine Ocular Manifestations of Albinism at eMedicine Imesch PD, Wallow IH, Albert DM; ... Aniridia is a congenital condition characterized by an extremely underdeveloped iris, which appears absent on superficial ...
*  FOXE3
2010). "Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia". Mol. Vis. 16: ...
*  Veronica van Heyningen
... and homeobox-containing gene from the aniridia region". Cell. 67 (6): 1059-74. doi:10.1016/0092-8674(91)90284-6. PMID 1684738 ...
*  Auditory processing disorder
April 2007). "Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation". Int J ...
*  Pax genes
"Homology of the eyeless gene of Drosophila to the small eye gene in mice and Aniridia in humans". Science. 265 (5173): 785-9. ...
*  Mary Fisher (swimmer)
She was born wiith the rare genetic condition aniridia, resulting in low vision which deteriorated as a teenager. She attended ...