Heterochromia Iridis Causes & Reasons

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Possible Causes

Glaucoma

Glaucoma is a group of eye diseases characterized by intraocular pressure-associated optic neuropathy. The two most common types are primary open-angle glaucoma and angle closure glaucoma. Patients suffering from glaucoma may present with a wide range of symptoms. Most commonly, they present with periorbital[…] [symptoma.com]

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Neuroblastoma

iridis (varying colors of the iris) hypertension from catecholamine production What Tests Should I Request to Confirm My Clinical Dx? [clinicaladvisor.com]

iridis: cervical, mediastinal neuroblastoma (prenatal / postnatal interruption of sympathetic tracts that mediate pigmentation of iris) Horner's syndrome (damage to sympathetic [pathologyoutlines.com]

[…] signs secretory diarrhea from production of vasoactive intestinal polypeptide (VIP), a paraneoplastic syndrome opsoclonus myoclonus ataxia, also a paraneoplastic syndrome heterochromia [clinicaladvisor.com]

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Piebaldism

iridis Different colored eyes 0001100 Intellectual disability Mental deficiency Mental retardation Mental retardation, nonspecific Mental-retardation [ more ] 0001249 Long [rarediseases.info.nih.gov]

iridis), white eye lashes, and wide-set inner corners of the eyes. [medicinenet.com]

Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and [arl4.library.sk]

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Nail-Patella Syndrome

The Nail-Patella syndrome (NPS) is an autosomal dominant connective-tissue disorder characterized by the absence or hypoplasia of the nails and patella, posterior illiac horns, elbow deformities, congenital nephropathy cervical ribs and eye problems. The presence of the posterior iliac horns is pathognomonic and have[…] [ncbi.nlm.nih.gov]

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Fuchs' Heterochromic Iridocyclitis

Most cases of heterochromia iridis are mild and do not have associated problems. What is heterochromia iridis? [medicinenet.com]

Heterochromia iridis-associated acquired Horner syndrome only occurs in children? 3. [neuro-ophthalmology.stanford.edu]

Affected people at times experience heterochromia iridis. [disabled-world.com]

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Klein-Waardenburg Syndrome

It is considered as a severe form of type 1, or classic Waardenburg syndrome, characterized by sensorineural hearing loss, dystopia canthorum, and heterochromia iridis. [symptoma.com]

Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and [hon.ch]

Moreover, heterochromia iridis (segmental or total and either unilateral or bilateral), skin and hair hypopigmentation, a white forelock, early graying of the hair (before [symptoma.com]

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Horner's Syndrome

iridis — may be present in congenital horner’s syndrome Lower eyelid reverse ptosis The eye may appear slightly bloodshot due to loss of vasoconstrictor activity in the vessels [lifeinthefastlane.com]

iridis Different colored eyes 0001100 Ipsilateral lack of facial sweating 0007451 Paralysis Inability to move 0003470 Showing of 6 Last updated: 12/1/2018 There are many [rarediseases.info.nih.gov]

If the onset of Horner syndrome is before two years of age, the colored portions of the eyes (irises) may be different colors (heterochromia iridis). [rarediseases.org]

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Congenital Deafness

iridis and pigmentary retinopathy. [symptoma.com]

iridis (two different-colored irises or two colors in the same iris), and hearing loss, while others may only have dystopia canthorum. [entnet.org]

iridis -- see above; or light blue eyes), and sensorineural deafness. [dizziness-and-balance.com]

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Iris Disorder

Most cases of heterochromia iridis are mild and do not have associated problems. What is heterochromia iridis? [medicinenet.com]

4/8/2015 Most cases of heterochromia iridis occur sporadically in people with no family history of heterochromia iridis. [rarediseases.info.nih.gov]

Heterochromia Iridis/Iridum Since infants are born with dark-colored eyes, you will not notice anything unusual until several months after your baby is born and his or her [eibnet1.com]

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Bee Sting

Corneal epithelial defect, corneal edema, secondary bacterial keratitis, heterochromia iridis, and internal ophthalmoplegia were identified The corneal edema markedly improved [ncbi.nlm.nih.gov]

Irreversible heterochromia-iridis, internal ophthalmoplegia, and punctate subcapsular lenticular opacities developed in a 9-year-old girl after she received a bee sting in [ncbi.nlm.nih.gov]

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Constipation

We identified a de novo nonsense mutation in SOX10 (p.G39X) in a female pediatric patient with Waardenburg syndrome with heterochromia iridis, profound bilateral sensorineural [ncbi.nlm.nih.gov]

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Panic Attacks

Iris pearls- seen in lepromatous uveitis Iris crystals Posterior synechiae Iris atrophy- seen in herpetic uveitis Heterochromia iridis Iris neovascularization Intraocular [eyewiki.aao.org]

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High Myopia-Sensorineural Deafness Syndrome

It consists of variable degrees of sensorineural hearing loss and pigmentary abnormalities of the skin, hair (white forelock), and eyes (heterochromia iridis). [quizlet.com]

iridis -- see above; or light blue eyes), and sensorineural deafness. [dizziness-and-balance.com]

iridis). [nature.com]

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Congenital Iris Coloboma

[…] iridium Heterochromia Iridum Heterochromia iridum, congenital Heterochromia Iridum, Waardenburg Syndrome Iris Bicolor, Heterochromia Iridis Uniocularis (see also:Systemic [atlasophthalmology.net]

[…] and Ciliary Body Case Coloboma of the Choroid, Optic Pit Coloboma of the Iris Coloboma of the Iris and the Ciiary Body Congenital, Bilateral Bridge-Coloboma of the Iris Heterochromia [atlasophthalmology.net]

Congenital Syndromes) Aniridia, Hereditary Coloboma of the Iris and Ciliary Body Case Coloboma of the Iris and the Ciiary Body Congenital, Bilateral Bridge-Coloboma of the Iris Heterochromia [atlasophthalmology.net]

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Autosomal Dominant Deafness 9

iridis (two different-colored irises or two colors in the same iris), and hearing loss, while others may only have dystopia canthorum. [entnet.org]

iridis -- see above; or light blue eyes), and sensorineural deafness. [dizziness-and-balance.com]

It consists of variable degrees of sensorineural hearing loss and pigmentary abnormalities of the skin, hair (white forelock), and eyes (heterochromia iridis). [consilieregenetica.org]

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Rubeosis Iridis

Iris douglasiana, flower essence Retinal Vein Occlusion Iris Pathological Dilatation Heterochromia Iridis Central Retinal Vein Occlusion References 2 Citations 1 References [meta.org]

[…] see HETEROCHROMIA IRIDIS, RUBEOSIS IRIDIS … Medical dictionary rubeosis — Reddish discoloration, as of the skin. [medicine.academic.ru]

Four patients with ischemic type of central or hemi-ce... read more Mentioned in this Paper Adenohypophyseal Diseases Entire Iris Rubeosis Iridis Pathologic Neovascularization [meta.org]

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Incontinentia Pigmenti Achromians

Treatment depends on the problems that are presented. 0008053 Delayed cranial suture closure 0000270 Heterochromia iridis Different colored eyes 0001100 Hypopigmented skin [rarediseases.info.nih.gov]

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Haddad Syndrome

Abstract Waardenburg syndrome (WS) is an autosomal dominant disease, characterized by dystopia canthorum, hyperplasia of the eyebrows, heterochromia iridis, white forelock [ncbi.nlm.nih.gov]

Waardenburg Syndrome Type I with Heterochromia Iridis and Circumscribed Hypopigmentation of the Skin. Pediatric Dermatology, Vol. 26, Issue. 6, p. 759. [cambridge.org]

iridis where the eyes are different colors, partial or fragmentary heterochromia iridis where blue is present in parts of the iris, and bright blue irises; (iii) hypochromic [spandidos-publications.com]

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Foreign Body in the Eye

Clinical manifestations include a rust-colored corneal stroma, heterochromia iridis, pupillary mydriasis, uveitis, cataract, lens subluxation, secondary glaucoma, and retinal [karger.com]

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Facial Nerve Paralysis of the Newborn

If Horner's syndrome persists, the infant may develop heterochromia iridis caused by failure of development of secondary pigmentation in the affected eye. [rrnursingschool.biz]

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Autosomal Dominant Deafness 28

iridis (two different-colored irises or two colors in the same iris), and hearing loss, while others may only have dystopia canthorum. [entnet.org]

It consists of variable degrees of sensorineural hearing loss and pigmentary abnormalities of the skin, hair (white forelock), and eyes (heterochromia iridis). [consilieregenetica.org]

[…] unusually wide bridge of the nose due to the inner angles of the eyes moved more sideways than they should be), white forelock (a white patch of hair in front of the head), heterochromia [entnet.org]

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Facial Hemiatrophy

iridis, Hemifacial atrophy, disturbed electrical signals accompanied with fast muscle spasm, Hemiatrophy of tongue and salivary gland, Achromia of the hair (lack of normally [pharmainfo.net]

iridis Refractive error Hemiatrophy of salivary gland and tongue Electrical disturbances which have a characteristic of fast muscle spasm Hemifacial atrophy Coup de sabre [syndromespedia.com]

Parry Romberg syndrome are as follows: Migraine, Facial pain, Hemianopia, Focal seizures, Hemiparesis, Cognitive impairment, Vomiting, Nausea, Enopthalmos, Refractive error, Heterochromia [pharmainfo.net]

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Panuveitis

Iris pearls- seen in lepromatous uveitis Iris crystals Posterior synechiae Iris atrophy- seen in herpetic uveitis Heterochromia iridis Iris neovascularization Intraocular [eyewiki.aao.org]

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Sarcoid Myocarditis

Heterochromia Iridis Heterochromia iridis is a rare condition that describes people with two different colored eyes. There are many potential... [medicinenet.com]

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Autosomal Dominant Deafness 33

iridis, a white forelock, leukoderma, and white eyelashes; and SNHL. [ajnr.org]

iridis -- see above; or light blue eyes), and sensorineural deafness. [dizziness-and-balance.com]

It consists of variable degrees of sensorineural hearing loss and pigmentary abnormalities of the skin, hair (white forelock), and eyes (heterochromia iridis). [consilieregenetica.org]

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Retinohepatoendocrinologic Syndrome

 Horner's syndrome, usually associated with heterochromia iridis (less common ). 49. ecchymosis of the eyelids heterochromia iridis 50.  Pheochromocytoma:  This rare [slideshare.net]

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Autosomal Dominant Deafness 56

iridis, a white forelock, leukoderma, and white eyelashes; and SNHL. [ajnr.org]

iridis). [nature.com]

iridis) Subtype characteristics: WS1. [ncbi.nlm.nih.gov]

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Familial Angiolipomatosis

iridis, partial, or segmental heterochromia (Figure 1a), which maybe unilateral or bilateral, and bilateral isohypochromia iridis (pale blue eyes).38, 40 Iris heterochromia [nature.com]

iridis, partial, or segmental heterochromia ( Figure 1a ), which maybe unilateral or bilateral, and bilateral isohypochromia iridis (pale blue eyes). 38, 40 Iris heterochromia [nature.com]

heterochromia iridis) arises when areas of the same iris are different in colour. [nature.com]

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Familial Isolated Dilated Cardiomyopathy

iridis, partial, or segmental heterochromia (Figure 1a), which maybe unilateral or bilateral, and bilateral isohypochromia iridis (pale blue eyes).38, 40 Iris heterochromia [nature.com]

heterochromia iridis) arises when areas of the same iris are different in colour. [nature.com]

Causes of heterochromia iridis with special reference to paralysis of the cervical sympathetics. [nature.com]

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Ocular Siderosis

Heterochromia iridis can be divided into those conditions which make the iris darker (hyperchromia) and those lighter (hypochromia). [mrcophth.com]

(Prussian blue-eosin, χ165.) within the iris and under the lens capsule, producing the clinical picture of heterochromia iridis (at least in unilateral cases) and of siderosis [kundoc.com]

In addition to heterochromia, there is decreased pupil lary activity due to precipitation of iron in the sphincter and dilator muscles. [kundoc.com]

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