Heterochromia Iridis: Causes & Reasons

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Possible Causes for Heterochromia Iridis

Piebaldism

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

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]

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

Waardenburg Syndrome Type 4C

(Sumber : MedicineNet ) WS adalah kelainan genetik yang menyebabkan tuli, rambut bagian depan berwarna putih, iris beda warna (heterochromia iridis), bulu mata berwarna putih [catatanmomkaki.blogspot.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 2A

iridis Hypoplastic iris stroma Abnormality of the integument Albinism Partial albinism Premature graying of hair Synophrys White eyebrow White eyelashes White forelock Ear [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]

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

Waardenburg Syndrome Type 4A

(Adams et al., Principles of Neurology, 6th ed, p272) Heterochromia iridis MedGen UID: 98395 •Concept ID: C0423318 • Finding Asymmetry between the two irides or asymmetry [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]

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

Waardenburg Syndrome Type 2D

[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]

Affiliated tissues include eye, and related phenotypes are heterochromia iridis and telecanthus Disease Ontology : 12 A Waardenburg's syndrome characterized by pigmentary [malacards.org]

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

Waardenburg Syndrome Type 2E

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

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

Sensorineural hearing loss occurs in the majority of people with WS2, and heterochromia iridis (differences in eye coloring) occurs in about half. [malacards.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]

Nail-Patella Syndrome

Abstract Nail-patella syndrome (NPS) is characterized by developmental defects of dorsal limb structures, nephropathy, and glaucoma and is caused by heterozygous mutations in the LIM homeodomain transcription factor LMX1B. In order to identify possible genotype-phenotype correlations, we performed LMX1B mutation[…] [ncbi.nlm.nih.gov]

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]

Horner's Syndrome

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

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]

A. von Passow: Okulare Paresen im Symptomenbilde des "Status dysraphicus", zugleich ein Beitrag zur Ätiologie der Sympathikusparese (Horner-Syndrom und Heterochromia iridis [whonamedit.com]

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]

iridis, white eyelashes, leukoderma and sometimes cochlear deafness. [medical-dictionary.thefreedictionary.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]

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]

Cervical Neuroblastoma

Horner syndrome was seen in five patients with accompanying heterochromia iridis in one. Five tumors had calcification. [link.springer.com]

McRae D, Shaw A (1979) Ganglioneuroma, heterchromia iridis, and Horner's syndrome. J Pediatr Surg 14: 612–614 PubMed Google Scholar 9. [link.springer.com]

Jaffe N, Cassady R, Filler RM, Peterson R, Traggis D (1975) Heterochromia and Horner syndrome associated with cervical and mediastinal neuroblastoma. [link.springer.com]

Waardenburg Syndrome

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

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

In 1951, Waardenburg defined 6 main features: (1) dystopia canthorum, (2) prominent broad nasal root, (3) synophrys, (4) white forelock, (5) heterochromia iridis, and (6) [medlink.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]

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 2C

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

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]

Waardenburg Syndrome Type 2B

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]

[…] the absence of dystopia canthorum (lateral displacement of the inner canthi of the eyes).[1][2]Sensorineural hearing loss occurs in the majority of people with WS2, and heterochromia [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

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]

Bagatelle-Cassidy Syndrome

iridis - Not a rare disease Heterotaxy HIBCH deficiency High molecular weight kininogen deficiency Hirschsprung disease type d brachydactyly Hirschsprung's disease His bundle [rarediseases.info.nih.gov]

Hereditary spherocytosis Hereditary vascular retinopathy Hermansky Pudlak syndrome 2 Hermansky-Pudlak syndrome Hernández-Aguirre Negrete syndrome Herpes simplex encephalitis Heterochromia [rarediseases.info.nih.gov]

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]

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]

Autosomal-Recessive Nonsyndromic Hearing Loss and Deafness DFNB61

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

Important features include branchial cleft pits, cysts or fistulae; preauricular pits; telecanthus; heterochromia iridis; white forelock; pigmentary anomalies; high myopia [geneticamedicala.org]