The author experienced a case of Aniridia in both eyes with increased intra-ouclar pressure. She was 3 month old and had no other congenital abnormalities and significant family history. Intra-ouclar pressure of her both eyes has been controlled within normal limits since goniopuncture was performed.
Aniridia* ; Congenital Abnormalities ; Humans ; Infant

The author experienced a case of Aniridia in both eyes with increased intra-ouclar pressure. She was 3 month old and had no other congenital abnormalities and significant family history. Intra-ouclar pressure of her both eyes has been controlled within normal limits since goniopuncture was performed.
Aniridia* ; Congenital Abnormalities ; Humans ; Infant

Most patients with Wilms tumor do not have associated congenital anomalies. However, significant associations with congenital urinary tract defects, hemihypertrophy, and sporadic aniridia have been reported. Horseshoe kidney is a congenital anomaly in which both kidneys are fused at the lower poles with renal parenchymal or fibrous isthmus. The risk of malignancy in a horseshoe kidney is probably not different from that in a normal kidney. But Wilms tumor are more common in patients with horseshoe kidney than in the general population. We report a case of Wilms tumor arising in a horseshoe kidney with brief review of related literatures.
Aniridia ; Humans ; Kidney* ; Urinary Tract ; Wilms Tumor*

The author have experienced a case of aniridia in a 44 year-old man. Aniridia is an uncommon congenital anomaly, is almost bilateral cmd appears as a dominant characteristic. Coincident anomalies are the rule, affectory especially the cornea and the lens. Chronic glaucoma is due to anatomical defect, with a reduction in the available filtration angle. It is noticeable, that very few patients with aniridia have retained good vision through a reasonably long life.
Adult ; Aniridia* ; Cornea ; Filtration ; Glaucoma ; Humans

No abstract available.
Aniridia ; Cerebellar Ataxia ; Esophageal Motility Disorders* ; Intellectual Disability

Complicated microphthalmos can be diagnosed when a reduction in global dimension is combined with other structural anomalies. These include corneal opacity or staphyloma, cataract, aniridia, corectopia, persistence of pupillary membrane or the tunica vasculosa lentis and hyaloid vessel, thickening or ossification of the choroid and various retinal anomalies. Complicated microphthalmos is frequently hereditary and the transmission may be either as an autosomal dominant or recessive or as a sex linked recessive trait. Four cases of bilateral complicated microphthalmos with cataract were found in a family.
Aniridia ; Cataract ; Choroid ; Corneal Opacity ; Humans ; Membranes ; Microphthalmos* ; Retinaldehyde

We implanted aniridia intraocular lenses (aniridia IOL) on three cases with complaint of glare caused by traumatic or congenital aniridias combined with cataract or aphakia. Aniridia IOLs were fixed by scleral fixation on one aphakia with traumatic aniridia, and at the ciliary sulcus on one aphakia with traumatic aniridia and one congenital aniridia with cataract. After follow-up of at least 2 months, visual improvement, absence of glare and cosmetic acceptance was observed without any complication in all cases.
Aniridia* ; Aphakia ; Cataract ; Follow-Up Studies ; Glare ; Lenses, Intraocular*

Microcornea is a condition characterized by a small cornea in an otherwise normal eye and can be defined when corneal diameter is less than 11.00mm. Microcornea may occur as an isolated abnormality or accompany other anterior segment anomalies like aniridia and anterior chamber cleavage abnormalities. Microcornea is part of nanophthalmos, a condition in which a reduction in global dimensions is the only structural abnormality, as well as microphthalmos, a term generally, used to signify a small, abnormal globe. Microcornea is a rare anomaly and its etiology is probably a primary aberration of the growth of the ectoderm of the optic cup. Both autosomal dominant and autosomal recessive patterns of inheritance occur, but it may appear sporadically. Cornea plana is usually seen in association with microcornea wherein the corneal curvature is less than normal. It is often associated with diffuse opacities of the cornea stroma. Cornea plana might be caused by a deep developmental arrest in the fourth month, at which time the cornea begins to increase its curvature relative to the sclera. The authors experienced a case of bilateral microcornea with cornea plana in a family which seemed to transmit as the dominant trait.
Aniridia ; Anterior Chamber ; Cornea* ; Ectoderm ; Humans ; Microphthalmos ; Sclera ; Wills

Microcornea is a condition characterized by a small cornea in an otherwise normal eye and can be defined when corneal diameter is less than 11.00mm. Microcornea may occur as an isolated abnormality or accompany other anterior segment anomalies like aniridia and anterior chamber cleavage abnormalities. Microcornea is part of nanophthalmos, a condition in which a reduction in global dimensions is the only structural abnormality, as well as microphthalmos, a term generally, used to signify a small, abnormal globe. Microcornea is a rare anomaly and its etiology is probably a primary aberration of the growth of the ectoderm of the optic cup. Both autosomal dominant and autosomal recessive patterns of inheritance occur, but it may appear sporadically. Cornea plana is usually seen in association with microcornea wherein the corneal curvature is less than normal. It is often associated with diffuse opacities of the cornea stroma. Cornea plana might be caused by a deep developmental arrest in the fourth month, at which time the cornea begins to increase its curvature relative to the sclera. The authors experienced a case of bilateral microcornea with cornea plana in a family which seemed to transmit as the dominant trait.
Aniridia ; Anterior Chamber ; Cornea* ; Ectoderm ; Humans ; Microphthalmos ; Sclera ; Wills

Aniridia or iridremis is a Clinical term denoting absence of the iris in whole or in part. Actually, total absence has not been reported, as there has been rudimentary iris tissue in all cases reported in the literature. Because of its extra ordinary propensities as a dominant characteristic, occasionally an irregular dominant, and because of its stricking appearance which facilitates investigation, it has received extensive study by geneticists. Indeed, so interesting are its hereditary and pathologic aspects that these have received for more attention that have therapeutic measures for aniridic cases. I have experienced a case of aniridic family, a 40 years old women and her two sons, without other disturbances during their life saving, except poor vision, which was not significant of in correction for visual acuity.
Adult ; Aniridia* ; Female ; Humans ; Iris ; Mothers* ; Visual Acuity