Colobomas
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A coloboma (from the Greek , meaning defect) is a hole in one of the structures of the eye, such as the
iris Iris most often refers to: *Iris (anatomy), part of the eye *Iris (mythology), a Greek goddess * ''Iris'' (plant), a genus of flowering plants * Iris (color), an ambiguous color term Iris or IRIS may also refer to: Arts and media Fictional ent ...
,
retina The retina (from la, rete "net") is the innermost, light-sensitive layer of tissue of the eye of most vertebrates and some molluscs. The optics of the eye create a focused two-dimensional image of the visual world on the retina, which then ...
,
choroid The choroid, also known as the choroidea or choroid coat, is a part of the uvea, the vascular layer of the eye, and contains connective tissues, and lies between the retina and the sclera. The human choroid is thickest at the far extreme rear ...
, or
optic disc The optic disc or optic nerve head is the point of exit for ganglion cell axons leaving the eye. Because there are no rods or cones overlying the optic disc, it corresponds to a small blind spot in each eye. The ganglion cell axons form the ...
. The hole is present from birth and can be caused when a gap called the choroid
fissure A fissure is a long, narrow crack opening along the surface of Earth. The term is derived from the Latin word , which means 'cleft' or 'crack'. Fissures emerge in Earth's crust, on ice sheets and glaciers, and on volcanoes. Ground fissure A ...
, which is present during early stages of prenatal development, fails to close up completely before a child is born. Ocular coloboma is relatively uncommon, affecting less than one in every 10,000 births. The classical description in medical literature is of a
keyhole A lock is a mechanical or electronic fastening device that is released by a physical object (such as a key, keycard, fingerprint, RFID card, security token or coin), by supplying secret information (such as a number or letter permutation or passw ...
-shaped defect. A coloboma can occur in one eye (unilateral) or both eyes (bilateral). Most cases of coloboma affect only the iris. The level of vision impairment of those with a coloboma can range from having no vision problems to being able to see only light or dark, depending on the position and extent of the coloboma (or colobomata if more than one is present).


Signs and symptoms

Visual effects may be mild to more severe depending on the size and location of the coloboma. If, for example, only a small part of the iris is missing, the vision may be normal; when a large part of the retina or (especially)
optic nerve In neuroanatomy, the optic nerve, also known as the second cranial nerve, cranial nerve II, or simply CN II, is a paired cranial nerve that transmits visual system, visual information from the retina to the brain. In humans, the optic nerve i ...
is missing, the vision may be poor. Commonly posterior colobomata affect the inferior retina, with resultant deficit in the superior visual field. Other conditions can be associated with a coloboma. Sometimes, the eye may be reduced in size, a condition called
microphthalmia Microphthalmia (Greek: grc, μικρός, mikros, small, label=none, grc, ὀφθαλμός, ophthalmos, eye, label=none, also referred as microphthalmos, is a developmental disorder of the eye in which one (unilateral microphthalmia) or both ( ...
.
Glaucoma Glaucoma is a group of eye diseases that result in damage to the optic nerve (or retina) and cause vision loss. The most common type is open-angle (wide angle, chronic simple) glaucoma, in which the drainage angle for fluid within the eye rem ...
,
nystagmus Nystagmus is a condition of involuntary (or voluntary, in some cases) eye movement. Infants can be born with it but more commonly acquire it in infancy or later in life. In many cases it may result in reduced or limited vision. Due to the invol ...
,
scotoma A scotoma is an area of partial alteration in the field of vision consisting of a partially diminished or entirely degenerated visual acuity that is surrounded by a field of normal – or relatively well-preserved – vision. Every normal mam ...
, or
strabismus Strabismus is a vision disorder in which the eyes do not properly align with each other when looking at an object. The eye that is focused on an object can alternate. The condition may be present occasionally or constantly. If present during a ...
may also occur.


Related conditions

Other ocular malformations that include coloboma or are related to it: *
CHARGE syndrome CHARGE syndrome (formerly known as CHARGE association) is a rare syndrome caused by a genetic disorder. First described in 1979, the acronym "CHARGE" came into use for newborn children with the congenital features of coloboma of the eye, heart ...
, a term that came into use as an
acronym An acronym is a word or name formed from the initial components of a longer name or phrase. Acronyms are usually formed from the initial letters of words, as in ''NATO'' (''North Atlantic Treaty Organization''), but sometimes use syllables, as ...
for the set of unusual congenital features seen in a number of newborn children. The letters stand for: oloboma of the eye, eart defects, tresia of the nasal
choanae The choanae (singular choana), posterior nasal apertures or internal nostrils are two openings found at the back of the nasal passage between the nasal cavity and the throat in tetrapods, including humans and other mammals (as well as crocodilia ...
, etardation of growth and/or development, enital and/or urinary abnormalities, and ar abnormalities and deafness. Although these features are no longer used in making a diagnosis, the name has remained. *
Cat eye syndrome Cat eye syndrome (CES) or Schmid–Fraccaro syndrome is a rare condition caused by an abnormal extra chromosome, i.e. a small supernumerary marker chromosome. This chromosome consists of the entire short arm and a small section of the long arm ...
, caused by the short arm (p) and a small section of the long arm (q) of human
chromosome 22 Chromosome 22 is one of the 23 pairs of chromosomes in human cell (biology), cells. Humans normally have two copies of chromosome 22 in each cell. Chromosome 22 is the second smallest human chromosome, spanning about 49 million DNA base pairs and ...
being present three (trisomic) or four times (tetrasomic) instead of the usual two times. The term "cat eye" was coined because of the particular appearance of the vertical colobomas in the eyes of some patients. *
Patau syndrome Patau syndrome is a syndrome caused by a chromosome, chromosomal abnormality, in which some or all of the Cell (biology), cells of the body contain Trisomy, extra genetic material from chromosome 13 (human), chromosome 13. The extra genetic mater ...
(trisomy 13), a chromosomal abnormality that can cause a number of deformities, some of which include structural eye defects, including microphthalmia,
Peters anomaly Anterior segment mesenchymal dysgenesis, or simply anterior segment dysgenesis (ASD), is a failure of the normal development of the tissues of the anterior segment of the eye. It leads to anomalies in the structure of the mature anterior segment, ...
,
cataract A cataract is a cloudy area in the lens of the eye that leads to a decrease in vision. Cataracts often develop slowly and can affect one or both eyes. Symptoms may include faded colors, blurry or double vision, halos around light, trouble w ...
, iris and/or fundus coloboma, retinal dysplasia or
retinal detachment Retinal detachment is a disorder of the eye in which the retina peels away from its underlying layer of support tissue. Initial detachment may be localized, but without rapid treatment the entire retina may detach, leading to vision loss and blin ...
, sensory
nystagmus Nystagmus is a condition of involuntary (or voluntary, in some cases) eye movement. Infants can be born with it but more commonly acquire it in infancy or later in life. In many cases it may result in reduced or limited vision. Due to the invol ...
,
cortical visual loss Cortical blindness is the total or partial loss of vision in a normal-appearing eye caused by damage to the brain's occipital cortex. Cortical blindness can be acquired or congenital, and may also be transient in certain instances. Acquired corti ...
, and
optic nerve hypoplasia Optic nerve hypoplasia (ONH) is a medical condition arising from the underdevelopment of the optic nerve(s). This condition is the most common congenital optic nerve anomaly. The optic disc appears abnormally small, because not all the optic nerve ...
. *
Treacher Collins syndrome Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. The degree to which a person is affected, however, may vary from mild to severe. Complications may include breathing prob ...
, autosomal dominant syndrome caused by mutation of ''
TCOF1 Treacle protein is a protein that in humans is encoded by the ''TCOF1'' gene. This gene encodes a nucleolar protein with an LIS1 homology domain. The protein is involved in ribosomal DNA gene transcription through its interaction with upstream b ...
''. Coloboma is part of a set of characteristic
facies In geology, a facies ( , ; same pronunciation and spelling in the plural) is a body of rock with specified characteristics, which can be any observable attribute of rocks (such as their overall appearance, composition, or condition of formatio ...
that features craniofacial malformations, such as downslanting eyes, ear anomalies, or hypoplasia of zygomatic bone and jaw (micrognathia). * Tilted disc syndrome, an unusual congenital malformation associated with
myopic Near-sightedness, also known as myopia and short-sightedness, is an eye disease where light focuses in front of, instead of on, the retina. As a result, distant objects appear blurry while close objects appear normal. Other symptoms may include ...
astigmatism Astigmatism is a type of refractive error due to rotational asymmetry in the eye's refractive power. This results in distorted or blurred vision at any distance. Other symptoms can include eyestrain, headaches, and trouble driving at nig ...
characterized by tilting of the intraocular tip of the optic nerve (the optic disc), also known as Fuchs coloboma.


Causes

Coloboma can be associated with a mutation in the ''
PAX2 Paired box gene 2, also known as Pax-2, is a protein which in humans is encoded by the ''PAX2'' gene. Function The Pax Genes, or Paired-Box Containing Genes, play important roles in the development and proliferation of multiple cell lines, dev ...
'' gene. Eye abnormalities have been shown to occur in over 90% of children with fetal alcohol syndrome.


Diagnosis

Typically a coloboma appears oval- or comet-shaped with round end towards the centre. There may be a few vessels (retinal or choroidal) at the edges. The surface may have irregular depression.


Treatment

Coloboma of the iris may be treated in a number of ways. A simple cosmetic solution is a specialized cosmetic contact lens with an artificial pupil aperture. Surgical repair of the iris defect is also possible. Surgeons can close the defect by stitching in some cases. Vision can be improved with glasses, contact lenses or even laser eye surgery but may be limited if the retina is affected or there is
amblyopia Amblyopia, also called lazy eye, is a disorder of sight in which the brain fails to fully process input from one eye and over time favors the other eye. It results in decreased vision in an eye that typically appears normal in other aspects. Amb ...
.


Epidemiology

The number of cases is around 5 to 7 per 100,000 births, making it a relatively rare condition.


Notable cases

Notable people with coloboma include actor
John Ritter Johnathan Southworth Ritter (September 17, 1948 – September 11, 2003) was an American actor. Ritter was a son of the singing cowboy star Tex Ritter and the father of actors Jason and Tyler Ritter. He is known for playing Jack Tripper on the ...
, model/actress
Karolina Wydra Karolina Wydra ( ; born March 5, 1981) is a Polish-American actress and model. She played Dominika Petrova on the Fox medical drama series '' House'', and vampire Violet Mazurski on the HBO dark fantasy series ''True Blood''. Wydra has starred ...
, ''
The New York Times ''The New York Times'' (''the Times'', ''NYT'', or the Gray Lady) is a daily newspaper based in New York City with a worldwide readership reported in 2020 to comprise a declining 840,000 paid print subscribers, and a growing 6 million paid ...
'' columnist
Andrew Ross Sorkin Andrew Ross Sorkin (born February 19, 1977) is an American journalist and author. He is a financial columnist for ''The New York Times'' and a co-anchor of CNBC's ''Squawk Box.'' He is also the founder and editor of DealBook, a financial news s ...
, tennis player
Arnaud Clément Arnaud Clément (; born 17 December 1977) is a French former professional tennis player and Davis Cup captain. Clément reached the final of the 2001 Australian Open and achieved a career-high ranking of world No. 10 in April of that year. Par ...
, pop singer songwriter Lachi, and
George Soros George Soros ( name written in eastern order), (born György Schwartz, August 12, 1930) is a Hungarian-American businessman and philanthropist. , he had a net worth of US$8.6 billion, Note that this site is updated daily. having donated mo ...
.
Madeleine McCann Madeleine Beth McCann (born 12 May 2003) is a British missing person who disappeared from her bed in a holiday apartment in Praia da Luz, Portugal, on the evening of 3 May 2007, at the age of 3. ''The Daily Telegraph'' described the disappeara ...
, a young girl who went missing in Portugal in 2007, does not have the condition. She has a freckle under her pupil. Her unique eye was a large part of her parents media appeal to find her.


References


External links


Micro & Anophthalmic Children's Society
{{Medical resources , ICD10 = {{ICD10, Q, 10, 3, q, 10, {{ICD10, Q, 12, 2, q, 10, {{ICD10, Q, 13, 0, q, 10, {{ICD10, Q, 14, 2, q, 10, {{ICD10, Q, 14, 8, q, 10 , ICD9 = {{ICD9, 377.23, {{ICD9, 743.4, {{ICD9, 743.46, {{ICD9, 743.52, {{ICD9, 743.57 , ICDO = , OMIM = 120200 , MedlinePlus = 003318 , eMedicineSubj = , eMedicineTopic = , DiseasesDB = 29894 , MeshID = D003103 Eye diseases Congenital disorders of eyes