Heterochromia Iridis: Causes & Reasons

Possible Causes for Heterochromia Iridis

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]

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

Waardenburg Syndrome Type 4B

Type I is characterized by the presence of dystopia canthorum, sensorineural hearing loss, heterochromia iridis, white forelock, hypopigmentation, and synophrys. [cureus.com]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

This is known as heterochromia iridis. Heterochromia can exist without the presence of Waardenburg syndrome. [healthline.com]

Waardenburg Syndrome Type 4C

Heterochromia iridis MedGen UID: 98395 •Concept ID: C0423318 • Finding Heterochromia iridis is a difference in the color of the iris in the two eyes. [ncbi.nlm.nih.gov]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

iridis Abnormality of the genitourinary system Cryptorchidism Abnormality of the integument Hypopigmented skin patches Premature graying of hair White eyebrow White eyelashes [ncbi.nlm.nih.gov]

Waardenburg Syndrome Type 2E

[from OMIM] Show allHide all Abnormality of the cardiovascular system Vascular dilatation Abnormality of the eye Blue irides Heterochromia iridis Hypopigmentation of the fundus [ncbi.nlm.nih.gov]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

iridis ; Heterogeneous ; Hypertonia ; Hypopigmentation of the fundus ; Hypopigmented skin patches ; Hypoplasia of the iris ; Hypoplasia of the semicircular canal ; Intellectual [mousephenotype.org]

Waardenburg Syndrome Type 2A

[from OMIM] Show allHide all Abnormality of head or neck Underdeveloped nasal alae Wide nasal bridge Abnormality of the eye Heterochromia iridis Hypoplastic iris stroma Abnormality [ncbi.nlm.nih.gov]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

A man aged 28-years represented with symptoms of mild unilateral hearing loss (right ear), complete heterochromia iridis, premature graying prior to 30 years of age, and synophrys [x-mol.com]

Waardenburg Syndrome Type 4A

iridis and brilliant blue eyes; congenital sensorineural hearing loss; and 'dystopia canthorum.' [ncbi.nlm.nih.gov]

Heterochromia iridis MedGen UID: 98395 •Concept ID: C0423318 • Finding Heterochromia iridis is a difference in the color of the iris in the two eyes. [ncbi.nlm.nih.gov]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

Waardenburg Syndrome Type 2D

Heterochromia iridis 0 EDN3 CL E G H 1908 613265 Waardenburg syndrome type 4B 613265 C2750457 OMIM 1 149 3178 131242 HP:0001100 HP:0001100 Heterochromia iridis 0 EDN3 CL [mseqdr.org]

[from OMIM] Show allHide all Abnormality of head or neck Telecanthus Abnormality of the eye Heterochromia iridis Ear malformation Congenital sensorineural hearing impairment [ncbi.nlm.nih.gov]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

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]

Glaucoma

We report a case of a 24-year-old male patient with post-laser assisted in situ keratomileusis (LASIK) culture-proven mycotic keratitis who developed pupillary block glaucoma on day 19 of medical management. The case was initially managed with multiple Nd-Yag peripheral iridotomy along with systemic and topical[…] [ncbi.nlm.nih.gov]

Horner's Syndrome

Okulare Paresen im Symptomenbilde des "Status dysraphicus", zugleich ein Beitrag zur Ätiologie der Sympathikusparese (Horner-Syndrom und Heterochromia iridis). [physio-pedia.com]

iridis) A lack of flushing on one side of their face on hot days or after playing Horner Syndrome Causes In about 35% to 40% of cases, doctors aren’t sure what exactly causes [webmd.com]

Von Passow’s syndrome is an association of Horner syndrome with heterochromia iridis. [whonamedit.com]

Nail-Patella Syndrome

Nail-patella syndrome is a rare hereditary disorder that results in abnormalities of the kidneys, bones, joints, toenails, and fingernails. Nail-patella syndrome is caused by a mutation of a gene that plays an important role in the development of limbs and kidneys. Commonly, people who have this syndrome are missing[…] [merckmanuals.com]

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]

Klein-Waardenburg Syndrome

Examination showed a depigmented macule (6 cm Χ 6 cm) on his forearm, white forelock, heterochromia iridis, dystopia canthorum, synophrys, and sensory neural deafness. [ijdvl.com]

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 [decs2020.bvsalud.org]

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]

There are a few well-known syndromes of which heterochromia iridis is a striking feature. [scientificamerican.com]

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]

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]

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]

Incontinentia Pigmenti Achromians

Ophthalmic associations can be variable like strabismus, aplasia/hypoplasia of iris, heterochromia iridis, corneal opacity, hypertelorism, myopia, uveal coloboma or microphthalmos [heraldopenaccess.us]

iridis, dacryostenosis, corneal opacities, optic atrophy, ptosis, nystagmus, myopia, and pigmentary disturbances of the fundus.2 The sole description of the ocular characteristics [healio.com]

iridis Different colored eyes 0001100 Hypopigmented skin patches Patchy loss of skin color 0001053 Seizures Seizure 0001250 Strabismus Cross-eyed Squint Squint eyes [ more [rarediseases.info.nih.gov]

Congenital Deafness with Total Albinism

Heterochromia iridis was a prominent feature in 1 sibship in which both segmental iris bicolor and complete heterochromia occurred. [albinismo.it]

Ocular Albinism with Late-Onset Sensorineural Deafness

Heterochromia iridis was a prominent feature in 1 sibship in which both segmental iris bicolor and complete heterochromia occurred. [albinismo.it]

Waardenburg Syndrome Type 2

The boy presented with heterochromia iridis and bilateral hearing loss, but did not show dystopia canthorum. [bmjopen.bmj.com]

Ocular examination revealed heterochromia iridum in four cases and heterochromia iridis in two cases (Figs. 1A, 1B, and 1D ). [healio.com]

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

Waardenburg Syndrome Type 2B

[from OMIM] Show allHide all Abnormality of head or neck Abnormality of the face Abnormality of the eye Heterochromia iridis Abnormality of the integument Premature graying [ncbi.nlm.nih.gov]

Affiliated tissues include eye and skin, and related phenotypes are sensorineural hearing impairment and heterochromia iridis Disease Ontology : 12 A Waardenburg's syndrome [malacards.org]

iridis (differences in eye coloring) occurs in about half.[1] Progressive hearing loss has also been reported in some people with WS2.[3] WS2 may be caused by changes (mutations [rarediseases.info.nih.gov]

Waardenburg Syndrome Type 1

Partial or complete heterochromia iridis occurs in 21-28 percent of patients with WS [5]. Our case had all these clinical findings. [escholarship.org]

The boy presented with heterochromia iridis and bilateral hearing loss, but did not show dystopia canthorum. [bmjopen.bmj.com]

Ocular examination revealed heterochromia iridum in four cases and heterochromia iridis in two cases (Figs. 1A, 1B, and 1D ). [healio.com]

Peripheral Demyelinating Neuropathy - Central Dysmyelination - Waardenburg Syndrome - Hirschsprung Disease

Waardenburg Syndrome

Partial or complete heterochromia iridis occurs in 21-28 percent of patients with WS [5]. Our case had all these clinical findings. [escholarship.org]

Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and [connects.catalyst.harvard.edu]

This is known as heterochromia iridis. Heterochromia can exist without the presence of Waardenburg syndrome. [healthline.com]

Congenital Horner Syndrome

iridis. [ncbi.nlm.nih.gov]

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

[…] syndrome, is related to heterochromia iridis and neuroblastoma. [malacards.org]

Pseudoretinitis Pigmentosa

Unilateral pigmentary degeneration of the retina associated with heterochromia iridis. [ncbi.nlm.nih.gov]

Waardenburg Syndrome Type 2C

Waardenburg syndrome is named after Petrus Johannes Waardenburg, a Dutch ophthalmologist, who noticed that heterochromia iridis often accompanied deafness. [dermnetnz.org]

Heterochromia iridis MedGen UID: 98395 •Concept ID: C0423318 • Finding Asymmetry between the two irides or asymmetry between different parts of one iris. [www-ncbi-nlm-nih-gov.ezproxy.u-pec.fr]

Hornova-Dlurosova Syndrome

iridis Heterotaxia autosomal dominant type Heterotaxy with polysplenia or asplenia Heterotaxy visceral X-linked Hexokinase deficiency hemolytic anemia HHV-6 encephalitis [personalizedcause.com]

B virus Herpetic embryopathy Herpetic keratitis Herrmann Opitz arthrogryposis syndrome Herrmann Opitz craniosynostosis Herrmann syndrome Hersh Podruch Weisskopk syndrome Heterochromia [personalizedcause.com]

Piebald Trait - Neurologic Defects Syndrome

More on Poikiloderma » Heterochromia iridis : Summary : Heterochromia iridis is a condition characterized by abnormalities of the iris (the colored part of the eye). [familydiagnosis.com]

iridis 60 33 occasional (7.5%) Occasional (29-5%) HP:0001100 12 aganglionic megacolon 60 33 occasional (7.5%) Occasional (29-5%) HP:0002251 13 neoplasm of the skin 60 33 [malacards.org]

iridis Different colored eyes 0001100 Neoplasm of the skin Skin tumors Tumor of the skin [ more ] 0008069 Percent of people who have these symptoms is not available through [rarediseases.info.nih.gov]