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Microcornea Wikipedia

Microcornea is a rare autosomal recessive congenital eye disease of calves worldwide. This disease is characterised by calves born with a small or absent cornea [2] . In cattle, microcornea is often associated with other diseases such as anasarca and bovine viral diarrhea microcornea. Definition from Wiktionary, the free dictionary. Jump to navigation Jump to search. English Etymology . micro-+‎ cornea. Noun . microcornea (plural microcorneas) A congenital defect of the eye in which the cornea is less that about 10 mm in diameter The cataract microcornea syndrome is a very rare congenital disease with a combination of congenital cataract and microcornea. The first description comes from 1952 by the American doctors M. Wallace Friedman and Edwinw S. Wright

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From Wikipedia, the free encyclopedia Microphthalmia (Greek: μικρός mikros = small; ὀφθαλμός ophthalmos = eye), also referred as microphthalmos, is a developmental disorder of the eye in which one (unilateral microphthalmia) or both (bilateral microphthalmia) eyes are abnormally small and have anatomic malformations Far-sightedness, also known as long-sightedness, hypermetropia, or hyperopia, is a condition of the eye where distant objects are seen clearly but near objects appear blurred. This blurred effect is due to incoming light being focused behind, instead of on, the retina wall due to insufficient accommodation by the lens. Small amount of hypermetropia in young patients is usually corrected by. Macrocephaly mental retardation facial dysmorphism. Macrocephaly mesodermal hamartoma spectrum. Macrocephaly mesomelic arms talipes. Macrocephaly pigmentation large hands feet. Macrocephaly short stature paraplegia. Macrodactyly of the foot. Macrodactyly of the hand. Macroepiphyseal dysplasia Mcalister Coe type

Wikipedia is a free online encyclopedia, created and edited by volunteers around the world and hosted by the Wikimedia Foundation microcornea An abnormally small cornea with a horizontal diameter of less than 10 mm. The condition is usually inherited, either as an autosomal dominant or autosomal recessive trait. It may be accompanied by hyperopia and glaucoma

This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources.Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine. Stub. An abnormally small cornea. * * * mi·cro·cor·nea kȯr nē ə n abnormal smallness of the cornea * * * mi·cro·cor·nea (mi″kro korґne ə) [micro + cornea] a usually bilateral developmental anomaly, in which the cornea is unusually smal Nanophthalmos is a rare genetic disease, included in the spectrum of developmental eye disorders, characterized by a small eye secondary to compromised growth[1]. Nanophthalmos is derived from the Greek word nano, meaning dwarf, and nanophthalmic eyes typically present very high to extreme axial hyperopia without other obvious structural defects[2] [3] Best vitelliform macular dystrophy (BVMD) First described by Adams in 1883, but named for Dr. Friedrich Best, who presented a detailed pedigree of the disease in 1905, Best vitelliform macular dystrophy, or Best disease, is a hereditary retinal dystrophy involving the retinal pigment epithelium (RPE), and leads to a characteristic bilateral yellow egg-yolk appearance of the macula

microcornea - Wiktionar

Cataract Microcornea Syndrome - zxc

  1. PubMed is a searchable database of medical literature and lists journal articles that discuss Microcornea corectopia macular hypoplasia. Click on the link to view a sample search on this topic. Click on the link to view a sample search on this topic
  2. ed abnormalities in the trabecular meshwork and anterior chamber angle resulting in elevated intraocular pressure (IOP), without other ocular or systemic developmental anomalies. Other terms have been used previously to describe this entity, including trabeculodysgenesis, goniodysgenesis and primary infantile.
  3. The fan-shaped cataract observed in the present family has not been reported before. [ncbi.nlm.nih.gov] Abnormal presentation of Peters' anomaly in a family with microcornea cataract syndrome Abstract A case of Peters' anomaly with bilateral crease on ear lobule and hypospadius was reported in a family with microcornea, cataract syndrome.. JP Medical Ltd, 31.03.2012 - 548 Seiten The.
  4. Peters' anomaly is one disease in a constellation of diseases that causes corneal opacity due to dysgenesis of the anterior segment during development. Peters' anomaly can cause devastating corneal opacity in an infant leading to severe amblyopia. Diagnosis involves careful anterior segment exam as well as testing for other systemic findings which would suggest Peters' Plus syndrome
  5. macrocornea: An X-linked recessive, nonprogressive enlargement of the cornea to 13 mm or greater, which is present at birth; 90% of cases occur in males. The cornea and the limbus are enlarged but histologically normal. Associated findings include anterior megalophthalmos, enlarged ciliary ring with zonular stretching (leading to.
  6. Microcornea or megalocornea • Anterior displaced Schwalbe's line (posterior embryotoxin) with attached iris strands • Smooth, cryptless iris surface with high iris insertion • Iris hypoplasia ranges from mild stromal thinning to hole formation, corectopia, and ectropion uveae • 50% associated glaucoma • Facial bone and teeth defects
  7. Laser peripheral iridotomy (also described as 'laser iridotomy' or simply termed 'iridotomy') is a medical procedure which uses a laser device to create a hole in the iris, thereby allowing aqueous humor to traverse directly from the posterior to the anterior chamber and, consequently, relieve a pupillary block

The ophthalmologist's role in the management and diagnosis of genetic disorders can be critical for patients, families and referring providers in the steadily advancing field of genetics. Genetic testing can be a useful medical tool in ophthalmology to help confirm or rule out a suspected inherited ocular disorder, provide important information of inheritance patterns and risk of recurrences. Mikrokornea. Eine Mikrokornea (aus griechisch μικρός mikros klein) ist eine zu kleine Hornhaut, also im Durchmesser unter 10 mm beim Erwachsenen und unter 8 mm beim Neugeborenen. Eine Mikrokornea findet sich bei der Mikrophthalmie (zu kleinen Augen), weiteren Entwicklungsstörungen des Auges sowie bei Fehlsichtigkeit Myopie Other ophthalmic features that can occur in patients with CHARGE syndrome include microphthalmia, microcornea, cataracts, strabismus, cranial nerve VII palsy, and ptosis. High refractive errors and amblyopia also occur in CHARGE syndrome. Cardiac Abnormalities. Cardiac malformations are found in 75-85% of patients with CHARGE syndrome Nanophthalmos is a rare genetic disease, included in the spectrum of developmental eye disorders, characterized by a small eye secondary to compromised growth[1]. Nanophthalmos is derived from the Greek word nano, meaning dwarf, and nanophthalmic eyes typically present very high to extreme axial hyperopia without other obvious structural defects[2] [3]

Occasionally microcornea, corneal opacity, glaucoma In addition, there may be a general developmental delay and a slight intellectual deficit. The combination of pronounced osteoporosis with spontaneous fractures together with the lack of an open large fontanel is considered to be an essential indicator of the geroderma osteodysplastica Morning glory syndrome is typically unilateral with equal involvement of the right and left eyes. Bilaterality of this condition can occur. 4 The visual prognosis is usually poor, in the 20/100 to 20/200 range. Serous retinal detachments can occur in 30% of individuals. Although not completely understood, it is postulated that there is a. Table 1 Advantages Disadvantages Scleral tunnel incision - Lower rates of endophthalmitis compared to CCI - Utilized in manual small incision cataract surgery (MSICS), which is more cost-effective than phacoemulsification in developing countries - Preferred method in microcornea-Preferred method in cases with low endothelial count - Requires conjunctival incision, which increases the risk of.

Microcornea 2. Megalocornea 3. Sclerocornea 4. Cornea plana 5. Keratectasia CONGENITAL CORNEAL ANOMALIES Microcornea • Very rare, hereditary, unilateral or bilateral • Corneal diameter is 10 mm or less • Shallow anterior chamber but other dimensions are normal Associated systemic syndromes Turner, Ehlers-Danlos, Weill-Marchesani and. cataract, juvenile, with microcornea and glucosuria A rare inherited condition (OMIM:612018) characterised by juvenile cataract with microcornea and renal glucosuria Persistent pupillary membrane represents remnants of anterior tunica vasculosa lentis. Embryologically, the iris forms as a solid sheet of mesodermal tissue known as the pupillary membrane. It is composed of vessels derived from anterior ciliary arteries and mesenchyme and lies ventral to the lens. The dorsal posterior hyaloid vessels. Wikipedia. Medical Information Search. English. English Español Português Français Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the A cataract is an opacity that develops in the crystalline lens of the eye Den grå stær microcornea syndrom er en meget sjælden medfødt sygdom med en kombination af medfødt katarakt og microcornea. Den første beskrivelse kommer fra 1952 af de amerikanske læger M. Wallace Friedman og Edwinw S. Wright

Microphthalmos - EyeWik

  1. Microcornea & Spontaneous Rupture of the Thoracic Aorta Symptom Checker: Possible causes include Ehlers-Danlos Syndrome. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search
  2. n/a Ensembl ENSG00000100122 n/a UniProt P53674 n/a RefSeq (mRNA) NM_001887 n/a RefSeq (protein) NP_001878 n/a Lleoliad (UCSC) n/a n/a PubMed search n/a Wicidata Gweld/Golygu Bod dynol Protein sy'n cael ei godio yn y corff dynol gan y genyn CRYBB1 yw CRYBB1 a elwir hefyd yn Crystallin beta B1 (Saesneg). Segment o DNA yw'r genyn , sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli.
  3. Kabuki syndrome (KS) also called Kabuki make-up syndrome is a a congenital malformation-mental retardation syndrome first described Niikawa et al and Kuroki et al ,two independent groups in Japan at the Journal of Pediatrics in 1981. Because its characteristic facial features resembled the make-up of actors in Kabuki, the traditional Japanese.
  4. Yemenite deaf-blind hypopigmentation syndrome is a condition caused by a mutation on the SRY-related HMG-box gene 10 (not SOX10).. It was characterized in 1990, after being seen in two siblings from Yemen who presented with a hitherto undescribed association of microcornea, colobomata of the iris and choroidea, nystagmus, severe early hearing loss, and patchy hypo- and hyperpigmentation
  5. Aniridia is the absence of the iris, usually involving both eyes. It can be congenital or caused by a penetrant injury. Isolated aniridia is a congenital disorder which is not limited to a defect in iris development, but is a panocular condition with macular and optic nerve hypoplasia, cataract, and corneal changes. Vision may be severely compromised and the disorder is frequently associated.

Schwartz Jampel syndrome (SJS) is a genetic disorder that affects bone and muscle development. Signs and symptoms may include muscle stiffness and weakness; joint deformities that affect mobility ( contractures ); short stature; small fixed facial features; and eye abnormalities. [1] Previously, SJS was divided into types 1 and 2 Mikrofon. Dari Wikipedia bahasa Indonesia, ensiklopedia bebas. Loncat ke navigasi Loncat ke pencarian. Mikrofon. Mikrofon ( bahasa Inggris: microphone) adalah suatu jenis transduser yang mengubah energi-energi akustik (gelombang suara) menjadi sinyal listrik. Mikrofon merupakan salah satu alat untuk membantu komunikasi manusia Congenital Clubfoot & Microcornea & Mitral Valve Insufficiency Symptom Checker: Possible causes include Ehlers-Danlos Syndrome. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search

Nance-Horan syndrome - Wikipedi

Eye problems may include coloboma, microcornea, and glaucoma. Wikipedia. Neurodevelopmental disorder. Neurodevelopmental disorders are a group of disorders which affect the development of the nervous system, leading to abnormal brain function which may affect emotion, learning ability, self-control, and memory.. Cataract-microcornea syndrome-Wikipedia. As he suffered from bilateral congenital cataracts his career was limited mainly to educational fields and research. Reginald John Gladstone-Wikipedia. Deprivation amblyopia (amblyopia ex anopsia) results when the ocular media become opaque, such as is the case with congenital cataract or corneal. The retinopathy of prematurity (RPM; Synonyms: retrolental fibroplasia (RLF) or retinopathy of prematurity, retinopathy of prematurity (ROP), Terry's syndrome) is due to the possibility of confusion with retinoblastoma and to the Pseudogliomen counted and is a retinal disease in preterm infants.The cause is the incomplete maturation (vascular supply) of the outer retina at birth in combination.

Aniridia - Wikipedi

Wikipedia. Micro syndrome. Rare autosomal recessive genetic disorder characterized by microcephaly, microcornea, congenital cataract, intellectual or developmental disability, optic atrophy, and hypogenitalism. The rare cases that have been examined are often within families, or the people that have cases of micro syndrome have a mutation in. Rare autosomal recessive genetic disorder characterized by microcephaly, microcornea, congenital cataract, intellectual or developmental disability, optic atrophy, and hypogenitalism. Wikipedia. Marden-Walker syndrome. Rare autosomal recessive congenital disorder. Characterized by blepharophimosis, microcephaly, micrognathia, multiple joint. Affected individuals in both of whose families also had microcornea and variable myopia. Conclusions This is the first report of mutations in GJA8 to be associated with autosomal dominant cataract and microcornea. Mutations in GJA8 cause 3.3% of congenital cataracts in the population of India. Citations & impact Wikipedia microdontia — n. a condition in which the teeth are unusually [universalium.academic.ru] 0000303 Microcornea Cornea of eye less than 10mm in diameter 0000482 Microdontia [rarediseases.info.nih.gov] Stomatitis. Turner's hypoplasia.

Microphthalmia - Wikipedi

Europe PMC is an archive of life sciences journal literature. A syndrome of mental retardation, microcephaly, a mongoloid slant to the palpebral fissures, microcornea, strabismus, myopia, optic atrophy, high-arched palate, preauricular skin tags and small mandible is described in four (including one set of twins) of seven sibs born to unaffected, nonconsanguineous parents of German ancestry Cataract microcornea syndrome Cataract, posterior polar, 1 Cataract, posterior polar, 3 Cataract, posterior polar, 4 Cataract, posterior polar, 5 Cataract, total congenital Centronuclear myopathy Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Cerebro-oculo-facio-skeletal syndrome Cerebrotendinous xanthomatosi The signs and symptoms of far-sightedness are blurry vision, headaches, and eye strain. The common symptom is eye strain. Difficulty seeing with both eyes (binocular vision) may occur, as well as difficulty with depth perception.Causes. Simple hypermetropia, the commonest form of hypermetropia is caused by normal biological variations in the development of eyeball Alagille syndrome is a genetic syndrome that can affect the liver and other parts of the body. The liver problems result from having fewer small bile ducts than normal in the liver. This leads to bile building-up inside the liver, which in turn causes liver scarring and damage. Signs and symptoms of Alagille syndrome are generally noticed in infancy or early childhood

Far-sightedness - Wikipedi

cataract, juvenile, with microcornea and glucosuria. A rare inherited condition (OMIM:612018) characterised by juvenile cataract with microcornea and renal glucosuria. Molecular pathology. Caused by defects of SLC16A12, which encodes a putative transporter highly expressed in the eye and kidney that catalyses the transmembrane transport of. Kyphoscoliotic Ehlers-Danlos syndrome (EDS) is caused by changes (mutations) in the PLOD1 gene, and, rarely, in the FKBP14 gene. This gene gives the body instructions to make (encodes) an enzyme that helps process molecules that allow collagen to form stable interactions with one another. Collagen is a protein that provides structure and strength to connective tissues throughout the body blepharoptosis. Wikipedia. Medical Information Search. symptoms hypergonadotropic hypogonadism cardiomyopathy dilated cardiomyopathy blepharoptosis broad nasal base mild intellectualblepharoptosis, skin lesions, and skeletal abnormalities are used as a reference to diagnosis this rare disease, and geneticblepharoptosis, and bone abnormalities, and occasionally marfanoid habitus (tall.

List of diseases (M) - Wikipedi

fanconi syndrome. Wikipedia. Medical Information Search. Paul SS, Saigal S Fanoconi's S. Fanconi's Syndrome.The effect of predniosolon and methyl testosterone and a review of the. In most cases, trisomy 18 is caused by having 3 copies of chromosome 18 in each cell in the body, instead of the usual 2 copies. The extra genetic material from the 3rd copy of the chromosome disrupts development, causing the characteristic signs and symptoms of the condition. About 5% of people with trisomy 18 have 'mosaic trisomy 18' (when there is an extra copy of the chromosome in only.

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WikiZero Özgür Ansiklopedi - Wikipedia Okumanın En Kolay Yolu . Far-sightedness, also known as long-sightedness, hypermetropia, or hyperopia, is a condition of the eye where distant objects are seen clearly but near objects appear blurred. This blurred effect is due to incoming light being focused behind, instead of on, the retina wall due to insufficient accommodation by the lens Katarakt-Mikrokornea-Syndrom. Das Katarakt-Mikrokornea-Syndrom ist eine sehr seltene angeborene Erkrankung mit einer Kombination von angeborene Katarakt und Mikrokornea. Die Erstbeschreibung stammt aus dem Jahre 1952 durch die US-amerikanischen Ärzte M. Wallace Friedman und Edwinw S. Wright

Microcornea definition of microcornea by Medical dictionar

Esta página se editó por última vez el 11 dic 2019 a las 21:39. El texto está disponible bajo la Licencia Creative Commons Atribución Compartir Igual 3.0; pueden aplicarse cláusulas adicionales.Al usar este sitio, usted acepta nuestros términos de uso y nuestra política de privacidad. Wikipedia® es una marca registrada de la Fundación Wikimedia, Inc., una organización sin ánimo de. Cataract-microcornea syndrome is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphis Microcornea, near-sightedness (myopia), glaucoma and detachment of the nerve-rich membrane in the back of the eye (retina) are common and can result in vision loss. Patients experiencing floaters, flashes or sudden curtains falling across their visual field should seek immediate medical attention. kEDS (formerly EDSVI) can be evident at birth Corneal Size Anomalies (Microcornea and Megalocornea) Corneal size anomalies are usually congenital and on the whole are rare. An abnormally small cornea (microcornea) has a diameter less than 10.0 mm). It usually causes severe hyperopia that in advanced age often predisposes the patient to angle closure glaucoma (see Table 10. 2) Colobomatous macrophthalmia with microcornea syndrome maps to the 2p23-p16 region. (PMID: 17506091) Elcioglu NH Akarsu NA (American journal of medical genetics. Part A 2007) 3; Colobomatous macrophthalmia with microcornea syndrome: report of a new pedigree. (PMID: 12900897) Toker E Ogut M (American journal of medical genetics. Part A.

Talk:Cataract-microcornea syndrome - Wikipedi

The front transparent region of the eye through which light passes may be small (microcornea) or the entire eye may appear unusually small (microphthalmia). The opening between the upper and lower eyelids (palpebral fissures) may be narrow and short (blepharophimosis), and the lids may have two or more rows of eyelashes Lowe syndrome is a rare genetic disorder that occurs almost exclusively in males. The prevalence is estimated to be between 1 and 10 males per 1,000,000 people. This condition has been reported in North and South America, Europe, Japan, and India

microcornea - medicine

The Nance-Horan syndrome (NHS) is a very rare congenital disease with a mainly occurring in males combination of congenital cataract, dental abnormalities and facial dysmorphia.. Synonyms are: English cataract, X-linked, with Hutchinsonian teeth; Mesiodens-cataract syndrome. The name refers to the (first) authors of the first descriptions, which were made independently of each other, from 1974. The Lenz microphthalmia syndrome or Lenz syndrome is an inherited disease with coloboma, missing or too small eye appendages, cataract in combination with various malformations of fingers, teeth, heart and urogenital tract.. Synonyms are: Lenz Dysmorphogenetic Syndrome; Lenz Syndrome II; Type I syndromic microphthalmia; The name refers to the German geneticist Widukind Lenz, who first. Eponymous terms. 130 female eponyms shared 156 eponymous terms, an average of 1.2 terms per author. The average number of eponymous terms per male author was 2.2 (7065/3374). The average date of publication of an eponyms first eponymous term was 1972 for females and 1891 for males Trichothiodystrophy (TTD) is a rare inherited, genetic disease characterized a broad spectrum of abnormalities. Patients with different manifestations are linked together by the common feature of short, dry, brittle, sulfur-deficient hair which has a characteristic tiger tail pattern under polarizing microscopy Right eye of a teenaged boy who was born with microcornea and cataracts and lost his left eye to complications of retinal detachment after glaucoma surgery in infancy. He developed glaucoma in his remaining eye in early childhood. Initially managed with glaucoma medications, he later required a drainage implant

Nanophthalmos - EyeWik

microphthalmos. Wikipedia. Medical Information Search. It may be associated with microphthalmos, cataracts, and increased intraocular pressure.Elongated ciliary processes are. Contact Lens Case Study Analysis. Contact lenses are a suitable substitute for correcting vision in a number of scenarios. There are hundreds of different contact lens types out there in today's market with the figure growing extensively every year. With the advancement of research and technology, manufactures are always attempting to better. Persistent hyperplastic primary vitreous (PHPV), also known as persistent fetal vasculature, is a congenital anomaly of the eye that results from failure of the embryological, primary vitreous, and the hyaloid vasculature to regress. It typically presents unilaterally, without associated systemic findings in normal full-term infants Preform History and Physical Examination to Determine if one of the following presen mi·cro·cosm (mī′krə-kŏz′əm) n. A small, representative system having analogies to a larger system in constitution, configuration, or development: He sees the auto industry as a microcosm of the U.S. itself (William J. Hampton). [Middle English microcosme, a human considered as a little universe, from Middle French, from Old French, from Late.

Best Disease and Bestrophinopathies - EyeWik

SOX10).It was characterized in 1990, after being seen in two siblings from Yemen who presented with a hitherto undescribed association of microcornea, colobomata of the iris and choroidea, nystagmus, severe early hearing loss, and patchy hypo- and hyperpigmentation [en.wikipedia.org]. Clinical description A brother and sister were described as having cutaneous patchy hypo- and. Retinal dysplasia is an eye disease affecting the retina of animals and, less commonly, humans. It is usually a nonprogressive disease and can be caused by viral infections, drugs, vitamin A deficiency, or genetic defects. Retinal dysplasia is characterized by folds or rosettes (round clumps) of the retinal tissue The Oculo-dento-digital dysplasia is a very rare congenital disease with abnormalities of the eye (okulo-), teeth (Dent) combined with malformations of the fingers or toes (digito).. Synonyms are: ODDD syndrome; ODD syndrome; Dysplasia, oculo-dento-osseous; Meyer-Schwickerath syndrome; English oculodentoosseous dysplasia (ODOD). The name refers to the first author of the first description from. Some had eye anomalies, including nystagmus, microcornea, myopia, hyperopia, and exotropia. Brain imaging was abnormal in all 4 patients who were studied: 3 had pituitary hypoplasia, 2 had hypothalamic hypoplasia, 2 had cortical atrophy, and 1 had delayed myelination. The 35-year-old also had central hypothyroidism and amenorrhea; brain imaging. Merle Pomeranian Dog Facts. The merle Pomeranian is a recent color pattern addition to the Pomeranian breed. Merle Pomeranians are not an accepted Pomeranian color pattern in many countries. Two merle Pomeranians should never be bred together. The merle gene modifies the base color of the dog's coat

Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family. Jamieson RV, Munier F, Balmer A, Farrar N, Perveen R, Black GC. Br J Ophthalmol, 87(4):411-412, 01 Apr 2003 Cited by: 21 articles | PMID: 12642301 | PMCID: PMC1771582. Free to rea Multiple-sclerosis & Spastic-quadriplegia Symptom Checker: Possible causes include Diffuse Cerebral Sclerosis of Schilder. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search alpha crystallins. Wikipedia. Medical Information Search. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered asAlpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: fourBeta-crystallin B3 is a protein that in humans is encoded by the CRYBB3 gene A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma. Br J Ophthalmol. 2003 Feb;87(2):197-202 microcopy. A photographic reproduction that is too small to be read without magnification. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, or visit the webmaster's page for free fun content

Angle closure glaucoma (ACG) is one of the leading causes of global blindness. Recent population based research on Chinese subjects in Singapore and a southern Indian population found high rates of ACG among those populations.12 Close to 2% of individuals over the age of 40 were found to have ACG in these studies. Given that almost half of the world's population lives in China and India. Congenital rubella syndrome (CRS) is the major complication associated with rubella infections. Measles infection of the mother during the first trimester of pregnancy is associated with encephalitis, hearing loss, and blindness in the newborn infant, and, later, intellectual disabilities. Between 1964 and 1965, a rubella epidemic resulted in. Aniridia is the absence of the iris, usually involving both eyes.It can be congenital or caused by a penetrant injury. [1] Isolated aniridia is a congenital disorder which is not limited to a defect in iris development, but is a panocular condition with macular and optic nerve hypoplasia, cataract, and corneal changes. [2] Vision may be severely compromised and the disorder is frequently. This report documents the most complex case of porcine congenital microphthalmic syndrome to the authors' knowledge, characterized by microphthalmia, multiple persistent pupillary membranes (PPMs) which consisted of both iris-to-iris and iris-to-lens, microphakia with cataract formation, myovascularised membrane in the vitreous, retinal detachment, and retinal dysplasia