Misdiagnosis of Hidden Causes of Nystagmus

Underlying conditions list:

The list of possible underlying conditions mentioned in various sources for Nystagmus includes:

• Normal vision - similar eye movements occur briefly after watching certain repeating patterns.
• Inner ear disturbances
• Labyrinthitis
• Meniere's disease
• Multiple sclerosis
• Stroke
• Brain tumor
• Alcoholism
• Drug abuse - some types
• See also causes of symptom Nystagmus
• Phencyclidine
• Babrbituartes
• Bilateral optic nerve hypoplasia
• Brain tumout
• Wernicke's encephalopathy
• Verloes-Deprez syndrome - nystagmus
• Spinocerebellar ataxia 28 - nystagmus
• Septo-Optic Dysplasia - nystagmus
• Opthalmoplegia progressive external scoliosis - nystagmus
• Hydroxyacyl-coa dehydrogenase, type 2, deficiency - nystagmus
• Hersh-Podruch-Weisskopk syndrome - nystagmus
• Ermine phenotype - nystagmus
• Episodic ataxia, type 2 - nystagmus
• Encephalitis, California serogroup viral - Nystagmus
• Corneal dystrophy - ichthyosis - microcephaly - mental retardation - nystagmus
• Chemical poisoning - Dinitrophenol - nystagmus
• Cerebro oculo skeleto renal syndrome - nystagmus
• Cerebellar hypoplasia - endosteal sclerosis - nystagmus
• Cerebellar degeneration - nystagmus
• Bardet-Biedl syndrome, type 2 - nystagmus
• Amaurosis congenita of Leber, type 3 - nystagmus
• Albinism - nystagmus
• Blue cone monochromatism
• Oxazepam
• Kallmann syndrome
• Phenytoin
• Inner ear tumor
• Cerebellar ataxia
• Lateral medullary syndrome
• Latent nystagmus
• Bilateral congenital cataract
• Spinocerebellar ataxia 29 - nystagmus
• Retinis pigmentosa - deafness - hypogenitalism - nystagmus
• Noonan Syndrome - nystagmus
• MOMO syndrome - nystagmus
• Minamata disease - nystagmus
• Macular dystrophy, retinal, 1, North Carolina type - nystagmus
• Incontinentia Pigmenti - nystagmus
• Hypomagnesemia primary - nystagmus
• Hypertrophic neuropathy of Dejerine-Sottas - nystagmus
• Fanconi pancytopenia - nystagmus
• Dandy-Walker - facial hemangioma - nystagmus
• Chromosome 8 recombinant syndrome - nystagmus
• Chromosome 11q duplication syndrome - nystagmus
• Bardet-Biedl syndrome, type 3 - nystagmus
• Arnold Stickler Bourne syndrome - nystagmus
• Amyloidosis, oculoleptomeningeal - nystagmus
• Amaurosis congenita of Leber, type 4 - nystagmus
• Alstrom syndrome - nystagmus
• Alcohol abuse - nystagmus
• Cardiofaciocutaneous syndrome - nystagmus
• Acoustic neuroma
• Ramsay Hunt syndrome
• Achromatopsia
• Abetalipoproteinaemia
• Ocular albinism type 1
• Down syndrome
• Barbiturates
• Arnold-Chiari malformation
• Trauma
• Alcohol
• X linked infantile nystagmus
• Nystagmus blockage syndrome
• Spinocerebellar ataxia 10 - nystagmus
• Sialuria, Finnish type - nystagmus
• Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis - nystagmus
• Phenytoin toxicity - nystagmus
• Night blindness, congenital stationary, type 2A - nystagmus
• Mental retardation - skeletal dysplasia - abducens palsy - nystagmus
• Luteinizing hormone releasing hormone, deficiency of, with ataxia - nystagmus
• Karandikar-Maria-Kamble syndrome - nystagmus
• Griscelli syndrome type II - nystagmus
• Francois dyscephalic syndrome - nystagmus
• Episodic ataxia, type 4 - nystagmus
• Chromosome 15q triplication syndrome - nystagmus
• Cerebelloparenchymal autosomal recessive disorder 3 - nystagmus
• Brown-Symmers disease - nystagmus
• Bardet-Biedl syndrome, type 4 - nystagmus
• Ataxia, spastic with congenital miosis - nystagmus
• Ataxia, Hereditary, Autosomal Dominant - nystagmus
• Amaurosis congenita of Leber, type 5 - nystagmus
• Amaurosis congenita of Leber, type 10 - nystagmus
• Adversive syndrome - nystagmus
• Adams Nance syndrome - nystagmus
• Posterior inferior cerebellar artery syndrome
• Chediak-Higashi disease
• Mèniére's disease
• Medications
• Spinocerebellar ataxia 11 - nystagmus
• Night blindness, congenital stationary, type 2B - nystagmus
• Methylcobalamin deficiency, cbl E complementation type - nystagmus
• Kaufman oculocerebrofacial syndrome - nystagmus
• Fitzsimmons-McLachlan-Gilbert syndrome - nystagmus
• Episodic ataxia, type 5 - nystagmus
• CRAPB - nystagmus
• Combarros Calleja Leno syndrome - nystagmus
• Chromosome 6, monosomy 6p23 - nystagmus
• Bone marrow failure - neurologic abnormalities - nystagmus
• Benign Paroxysmal Positional Vertigo - Nystagmus
• Bardet-Biedl syndrome, type 5 - nystagmus
• Bardet-Biedl syndrome, type 10 - nystagmus
• Aniridia, sporadic - nystagmus
• Amaurosis congenita of Leber, type 6 - nystagmus
• Amaurosis congenita of Leber, type 11 - nystagmus
• Adrenoleukodystrophy, autosomal, neonatal form - nystagmus
• Abetalipoproteinemia - nystagmus
• Lowry-Wood syndrome
• Glomus jugulare tumor
• Lorazepam
• X-linked cone-rod dystrophy
• Thiamine (Vitamin B1) deficiency
• Trochlear neve malfunction
• Benzodiazepines
• Persistent tunica vasculosa lentis
• Volubilis, syndrome du - nystagmus
• Spinocerebellar ataxia 12 - nystagmus
• Spastic paraplegia 7, autosomal recessive - nystagmus
• Neurofibromatosis-Noonan syndrome - nystagmus
• Lissencephaly with cerebellar hypoplasia, recessive - nystagmus
• Infantile sialic acid storage disorder - nystagmus
• GM1 gangliosidosis - nystagmus
• Gangliosidosis generalized GM1, type 1 - nystagmus
• Donepezil toxicity - nystagmus
• Céstan-Chenais syndrome - nystagmus
• Chromosome 8p deletion syndrome - nystagmus
• Cerebellar ataxia, X-linked - nystagmus
• Bardet-Biedl syndrome, type 6 - nystagmus
• Bardet-Biedl syndrome, type 11 - nystagmus
• Amaurosis congenita of Leber, type 7 - nystagmus
• 18p minus syndrome - nystagmus
• Gabapentin
• Klippel-Feil syndrome
• Decompression sickness
• Vestibular neuronitis
• Heat stroke
• Pituitary tumour
• Congenital
• Superior canal dehiscence syndrome
• WAGR Syndrome - nystagmus
• Urban Schosser Spohn syndrome - Nystagmus
• Spinocerebellar ataxia, X-linked, 5 - nystagmus
• Spinocerebellar ataxia 13 - nystagmus
• Red skin pigment anomaly of New Guinea - nystagmus
• Ophthalmoplegia, progressive external - scoliosis - nystagmus
• Oculo-osteo-cutaneous syndrome - nystagmus
• Microcephaly - mental retardation - retinopathy - nystagmus
• Erythrokeratodermia with ataxia - nystagmus
• Dobrow syndrome - nystagmus
• Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss - nystagmus
• Caudal appendage - deafness - nystagmus
• Cataract, microphthalmia and nystagmus - nystagmus
• Bardet-Biedl syndrome, type 7 - nystagmus
• Bardet-Biedl syndrome, type 12 - nystagmus
• Ataxia tapetoretinal degeneration - nystagmus
• Amaurosis congenita of Leber, type 8 - nystagmus
• Ethotoin
• Syringobulbia
• Rufous oculocutaneous albinism
• Lithium
• Syphilis
• Lysergic acid diethyamide
• Horner syndrome
• Tullio phenomenon
• Familial
• Spinocerebellar ataxia, autosomal dominant - nystagmus
• Proud-Levine-Carpenter syndrome - nystagmus
• Pena-Shokeir syndrome Type 2 - nystagmus
• Optic pathway glioma - nystagmus
• OFD syndrome type 8 - nystagmus
• Oculopalatoskeletal syndrome - nystagmus
• Oculocerebral hypopigmentation syndrome, type Preus - nystagmus
• Meier-Blumberg-Imahorn syndrome - nystagmus
• Marinesco-Sjogren syndrome - nystagmus
• Hepatic encephalopathy syndrome - nystagmus
• Hajdu-Cheney Syndrome - nystagmus
• Fabry's Disease - nystagmus
• Cerebrorenodigital syndrome - nystagmus
• Branchio-skeleto-genital syndrome - nystagmus
• Bardet-Biedl syndrome, type 8 - nystagmus
• Bardet-Biedl Syndrome - nystagmus
• Arthritis - short stature - deafness - nystagmus
• Arima syndrome - nystagmus
• Amaurosis congenita of Leber, type 9 - nystagmus
• Absence of septum pellucidum and septo-optic dysplasia - nystagmus
• Oculocutaneous albinism type 3
• Vertebrobasilar dolichoectasia
• Parinaud syndrome
• Thalamic emorrhage
• Tacrine toxicity - nystagmus
• Spinocerebellar ataxia 15 - nystagmus
• Osteosclerosis, abnormalities of nervous system and meninges - nystagmus
• Krause-Kivlin syndrome - nystagmus
• Homocystinuria due to defect in methylation cbl e - nystagmus
• Craniofacial dysostosis type 1 - nystagmus
• Chromosome 18 deletion syndrome - nystagmus
• Chromosome 10, trisomy 10pter p13 - nystagmus
• Chorioretinal atrophy, progressive bifocal - nystagmus
• Bonnier's syndrome - nystagmus
• Bardet-Biedl syndrome, type 9 - nystagmus
• Auriculoocular anomalies - cleft lip - nystagmus
• Arnold-Chiari malformation type 3 - nystagmus
• Ablinism I syndrome - nystagmus
• Miner's nystagmus
• Temazepam
• Usher's syndrome
• Diazepam
• Oculocutaneous albinism type 4
• Inner ear infection
• Brain cyst (see Brain tumor)
• Head trauma
• Ischemic lesions of the labyrinth
• Ischemic lesions of the vestibular nerve
• Encephalopathy
• Rod monochromatism
• Wernicke-Korsakoff syndrome - Nystagmus
• Spinocerebellar ataxia 25 - nystagmus
• Spinocerebellar ataxia 16 - nystagmus
• Spastic paraplegia 16, X-linked - nystagmus
• Singh-Chhaparwal-Dhanda syndrome - nystagmus
• Sialidosis type 1 and 3 - nystagmus
• Retinal dysplasia, X-linked - nystagmus
• Retinal degeneration - nanophthalmos - glaucoma - nystagmus
• Pellagra-like syndrome - nystagmus
• Olivopontocerebellar atrophy - deafness - nystagmus
• Ocular albinism - nystagmus
• Forsius-Eriksson syndrome - nystagmus
• Fanconi-Turler syndrome - nystagmus
• Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy - nystagmus
• Cataract and cardiomyopathy - nystagmus
• Babinski-Nageotte syndrome - nystagmus
• Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities - nystagmus
• Arnold-Chiari malformation type 4 - nystagmus
• Aniridia - ptosis - mental retardation - obesity, familial - nystagmus
• Ampola syndrome - nystagmus
• Amaurosis hypertrichosis - nystagmus
• Absence of septum pellucidum with porencephalia syndrome - nystagmus
• Cerebellar syndrome
• Inner ear inflammation
• Head injury
• Encephalitis
• Acute labyrinthitis
• Thiamine deficiency
• Bilateral optic nerve nystagmus
• Idiopathic
• Zonular cataract and nystagmus - Nystagmus
• Yemenite deaf-blind hypopigmentation syndrome - Nystagmus
• Wilkie Taylor Scambler syndrome - Nystagmus
• Wallenberg's Syndrome - Nystagmus
• Unusual facies, hepatic fibrosis, renal cysts and mental retardation - nystagmus
• Spinocerebellar ataxia 26 - nystagmus
• Spinocerebellar ataxia 17 - nystagmus
• Spinocerebellar ataxia - dysmorphism - nystagmus
• Sphingolipidosis - nystagmus
• Richieri Costa Guion-Almeida syndrome - nystagmus
• Pseudoadrenoleukodystrophy - nystagmus
• Paraneoplastic cerebellar degeneration - nystagmus
• Neuronal intranuclear inclusion disease - nystagmus
• Neuroaxonal dystrophy - renal tubular acidosis - nystagmus
• Mental retardation, Mietens-Weber type - nystagmus
• Homocystinuria due to defect in methylation (cbl g) - nystagmus
• Hemiplegic migraine, familial type 1 - nystagmus
• Griscelli disease - nystagmus
• Congenital disorder of glycosylation type 1/IIX - nystagmus
• Coloboma chorioretinal cerebellar vermis aplasia - nystagmus
• Chromosome 6 ring syndrome - nystagmus
• Brachmann-De Lange Syndrome - nystagmus
• Borjeson Syndrome - nystagmus
• Ataxia spastic congenital miosis - nystagmus
• Amaurosis congenita of Leber, type 1 - nystagmus
• Achromatopsia incomplete, X-linked - nystagmus
• Acanthocytosis - nystagmus
• Oculocutaneous albinism (tyrosinase negative)
• Brain bleed (see Stroke symptoms)
• Vertigo
• Ketamine
• Spinocerebellar ataxia 27 - nystagmus
• Spastic paraplegia 2, X-linked - nystagmus
• Retinitis pigmentosa - mental retardation - deafness - nystagmus
• Pierson syndrome - nystagmus
• Phillips-Griffiths syndrome - nystagmus
• Pelizaeus-Merzbacher Disease - nystagmus
• Optic atrophy, idiopathic, autosomal recessive - nystagmus
• OFD syndrome type IX - nystagmus
• Manz syndrome - nystagmus
• Hypomyelination - hypogonadotropic hypogonadism - hypodontia - nystagmus
• Cockayne syndrome - nystagmus
• Chromosome 18q, partial deletion - nystagmus
• Chromosome 10p duplication syndrome - nystagmus
• Cerebral abscess - nystagmus
• Cerebellar abscess - nystagmus
• Bardet-Biedl syndrome, type 1 - nystagmus
• Amaurosis congenita of Leber, type 2 - nystagmus
• Clonazepam
• Cerebrovascular accident
• Koerber-Salus-Elshnig syndrome
• Ethanol
• Congenital stationary night blindness
• Cholesteatoma
• Friedreich's ataxia
• Brain abscess
• Cerebrovascualr accident (see Stroke symptoms)
• Benign positional vertigo

Nystagmus as a symptom:

Conditions listing Nystagmus as a symptom may also be potential underlying conditions.

For a more detailed analysis of Nystagmus as a symptom, including causes, drug side effect causes, and drug interaction causes, please see our Symptom Center information for Nystagmus.

• 18p minus syndrome
• 3-
• 8p-Syndrome, partial
• Abetalipoproteinemia
• Ablinism I syndrome
• Absence of septum pellucidum and septo-optic dysplasia
• Absence of septum pellucidum with porencephalia syndrome
• Acanthocytosis
• Achromatopsia
• Achromatopsia incomplete, X-linked
• Adams Nance syndrome
• Adrenoleukodystrophy, autosomal, neonatal form
• Adversive syndrome
• Albinism
• Alcohol abuse
• Alstrom syndrome
• Amaurosis congenita of Leber, type 1
• Amaurosis congenita of Leber, type 10
• Amaurosis congenita of Leber, type 11
• Amaurosis congenita of Leber, type 2
• Amaurosis congenita of Leber, type 3
• Amaurosis congenita of Leber, type 4
• Amaurosis congenita of Leber, type 5
• Amaurosis congenita of Leber, type 6
• Amaurosis congenita of Leber, type 7
• Amaurosis congenita of Leber, type 8
• Amaurosis congenita of Leber, type 9
• Amaurosis hypertrichosis
• Ampola syndrome
• Amyloidosis, oculoleptomeningeal
• Aniridia
• Aniridia - ptosis - mental retardation - obesity, familial
• Aniridia ptosis mental retardation obesity familial type
• Aniridia, sporadic
• Arima syndrome
• Arnold Stickler Bourne syndrome
• Arnold-Chiari malformation type 3
• Arnold-Chiari malformation type 4
• Arthritis - short stature - deafness
• Ataxia spastic congenital miosis
• Ataxia tapetoretinal degeneration
• Ataxia, Hereditary, Autosomal Dominant
• Ataxia, spastic with congenital miosis
• Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities
• Auriculoocular anomalies - cleft lip
• Babinski-Nageotte syndrome
• Bardet-Biedl Syndrome
• Bardet-Biedl syndrome, type 1
• Bardet-Biedl syndrome, type 10
• Bardet-Biedl syndrome, type 11
• Bardet-Biedl syndrome, type 12
• Bardet-Biedl syndrome, type 2
• Bardet-Biedl syndrome, type 3
• Bardet-Biedl syndrome, type 4
• Bardet-Biedl syndrome, type 5
• Bardet-Biedl syndrome, type 6
• Bardet-Biedl syndrome, type 7
• Bardet-Biedl syndrome, type 8
• Bardet-Biedl syndrome, type 9
• Benign Paroxysmal Positional Vertigo
• Biemond Syndrome
• Bone marrow failure - neurologic abnormalities
• Bonnier's syndrome
• Borjeson Syndrome
• Brachmann-De Lange Syndrome
• Brachydactyly nystagmus cerebellar ataxia
• Branchio-skeleto-genital syndrome
• Brown-Symmers disease
• Cardiofaciocutaneous Syndrome
• Cataract - intellectual deficit - anal atresia - urinary defects
• Cataract and cardiomyopathy
• Cataract, microphthalmia and nystagmus
• Caudal appendage - deafness
• Cerebellar abscess
• Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss
• Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss
• Cerebellar ataxia, X-linked
• Cerebellar degeneration
• Cerebellar hypoplasia - endosteal sclerosis
• Cerebellar hypoplasia - tapetoretinal degeneration
• Cerebelloparenchymal autosomal recessive disorder 3
• Cerebral abscess
• Cerebro oculo skeleto renal syndrome
• Cerebrorenodigital syndrome
• Chediak-Higashi like syndrome
• Chemical poisoning - Acrylamide
• Chemical poisoning - Bromide
• Chemical poisoning - Carbon Disulfide
• Chemical poisoning - Chloroform
• Chemical poisoning - Dinitrophenol
• Chemical poisoning - Ethylene Oxide
• Chemical poisoning - Glufosinate
• Chemical poisoning - Glyphosate
• Chemical poisoning - Manganese
• Chemical poisoning - Methanol
• Chemical poisoning - Methyl Bromide
• Chemical poisoning - Monosodium Methanarsenate
• Chemical poisoning - Sodium Monofluoroacetate
• Chemical poisoning - Toluene Diisocyanate
• Chemical poisoning - Trichloroethylene
• Chemical poisoning - Xylene
• Chorioretinal atrophy, progressive bifocal
• Chromosome 10, trisomy 10p
• Chromosome 10, trisomy 10pter p13
• Chromosome 10p duplication syndrome
• Chromosome 11, deletion 11p
• Chromosome 11q duplication syndrome
• Chromosome 15q triplication syndrome
• Chromosome 18 deletion syndrome
• Chromosome 18q, partial deletion
• Chromosome 6 ring syndrome
• Chromosome 6, monosomy 6p23
• Chromosome 8 recombinant syndrome
• Chromosome 8, Monosomy 8p2
• Chromosome 8, Monosomy 8p21-pter
• Chromosome 8, monosomy 8q
• Chromosome 8p deletion syndrome
• Chromosome 8p duplication syndrome
• Cockayne syndrome
• Coloboma chorioretinal cerebellar vermis aplasia
• Combarros Calleja Leno syndrome
• Congenital disorder of glycosylation type 1/IIX
• Corneal dystrophy - ichthyosis - microcephaly - mental retardation
• Corneal dystrophy - perceptive deafness
• Craniofacial dysostosis type 1
• CRAPB
• Céstan-Chenais syndrome
• Dandy-Walker - facial hemangioma
• Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
• Dandy-Walker Syndrome
• De Grouchy Syndrome
• Deletion 11p
• Deletion 18q
• Deletion 8q
• Diabetes insipidus, diabetes mellitus, optic atrophy
• Diabetes insipidus, diabetes mellitus, optic atrophy, deafness, mitochondrial form
• DIDMOAD Syndrome, Mitochondrial form
• Dobrow syndrome
• Donepezil toxicity
• Duplication 10p
• Encephalitis, California serogroup viral
• Episodic ataxia, type 2
• Episodic ataxia, type 4
• Episodic ataxia, type 5
• Ermine phenotype
• Erythrokeratodermia with ataxia
• Fabry's Disease
• Fanconi pancytopenia
• Fanconi-Turler syndrome
• Fitzsimmons-McLachlan-Gilbert syndrome
• Forsius-Eriksson syndrome
• Francois dyscephalic syndrome
• Gangliosidosis generalized GM1, type 1
• GM1 gangliosidosis
• Griscelli disease
• Griscelli syndrome type II
• Hajdu-Cheney Syndrome
• Hemiplegic migraine, familial type 1
• Hepatic encephalopathy syndrome
• Hersh-Podruch-Weisskopk syndrome
• Homocystinuria due to defect in methylation (cbl g)
• Homocystinuria due to defect in methylation cbl e
• Hydroxyacyl-coa dehydrogenase, type 2, deficiency
• Hypertrophic neuropathy of Dejerine-Sottas
• Hypomagnesemia primary
• Hypomyelination - hypogonadotropic hypogonadism - hypodontia
• Incontinentia Pigmenti
• Infantile Refsum Disease
• Infantile sialic acid storage disorder
• Karandikar-Maria-Kamble syndrome
• Kaufman oculocerebrofacial syndrome
• Krause-Kivlin syndrome
• Labrynthitis
• Lissencephaly with cerebellar hypoplasia, recessive
• Luteinizing hormone releasing hormone, deficiency of, with ataxia
• Macular dystrophy, retinal, 1, North Carolina type
• Manz syndrome
• Marinesco-Sjogren syndrome
• Meier-Blumberg-Imahorn syndrome
• Mental retardation - blepharophimosis - obesity - web neck
• Mental retardation - macrocephaly - coarse facies - hypotonia
• Mental retardation - skeletal dysplasia - abducens palsy
• Mental retardation unusual facies ampola type
• Mental retardation, Mietens-Weber type
• Methylcobalamin deficiency, cbl E complementation type
• Microcephaly - mental retardation - retinopathy
• Microcephaly - microphthalmos - blindness
• Minamata disease
• MOMO syndrome
• N syndrome
• Neuroaxonal dystrophy - renal tubular acidosis
• Neurofibromatosis-Noonan syndrome
• Neuronal intranuclear inclusion disease
• Night blindness, congenital stationary, type 2A
• Night blindness, congenital stationary, type 2B
• Noonan Syndrome
• Ocular albinism
• Oculo-osteo-cutaneous syndrome
• Oculocerebral hypopigmentation syndrome, type Preus
• Oculopalatoskeletal syndrome
• OFD syndrome type 8
• OFD syndrome type IX
• Olivopontocerebellar atrophy - deafness
• Ophthalmoplegia, progressive external - scoliosis
• Opthalmoplegia progressive external scoliosis
• Optic atrophy, idiopathic, autosomal recessive
• Optic pathway glioma
• Osteosclerosis, abnormalities of nervous system and meninges
• Paraneoplastic cerebellar degeneration
• Pelizaeus-Merzbacher Disease
• Pellagra-like syndrome
• Pena-Shokeir syndrome Type 2
• Phenytoin toxicity
• Phillips-Griffiths syndrome
• Pierson syndrome
• Polydactyly cleft lip palate psychomotor retardation
• Proud-Levine-Carpenter syndrome
• Pseudoadrenoleukodystrophy
• Red skin pigment anomaly of New Guinea
• Refsum Disease
• Retinal degeneration - nanophthalmos - glaucoma
• Retinal dysplasia, X-linked
• Retinis pigmentosa - deafness - hypogenitalism
• Retinitis pigmentosa - mental retardation - deafness
• Revesz Syndrome
• Richieri Costa Guion-Almeida syndrome
• Robinow-Unger syndrome
• SCHAD deficiency
• Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
• Septo-Optic Dysplasia
• Sialidosis type 1 and 3
• Sialuria, Finnish type
• Singh-Chhaparwal-Dhanda syndrome
• Spastic paraplegia 16, X-linked
• Spastic paraplegia 2, X-linked
• Spastic paraplegia 7, autosomal recessive
• Sphingolipidosis
• Spinocerebellar ataxia - dysmorphism
• Spinocerebellar ataxia 10
• Spinocerebellar ataxia 11
• Spinocerebellar ataxia 12
• Spinocerebellar ataxia 13
• Spinocerebellar ataxia 15
• Spinocerebellar ataxia 16
• Spinocerebellar ataxia 17
• Spinocerebellar ataxia 25
• Spinocerebellar ataxia 26
• Spinocerebellar ataxia 27
• Spinocerebellar ataxia 28
• Spinocerebellar ataxia 29
• Spinocerebellar ataxia, autosomal dominant
• Spinocerebellar ataxia, X-linked, 5
• Split hand split foot nystagmus
• Tacrine toxicity
• Type 10 17b-hydroxysteroid dehydrogenase deficiency
• Unusual facies, hepatic fibrosis, renal cysts and mental retardation
• Urban Schosser Spohn syndrome
• Verloes-Deprez syndrome
• Volubilis, syndrome du
• WAGR Syndrome
• Wallenberg's Syndrome
• Wernicke-Korsakoff syndrome
• Wilkie Taylor Scambler syndrome
• Wilms tumor - aniridia - genitourinary anomalies - mental retardation
• Wolfram Syndrome 2
• Wolfram Syndrome, Mitochondrial form
• X-linked mental retardation - hypotonia
• Yemenite deaf-blind hypopigmentation syndrome
• Zonular cataract and nystagmus

About underlying conditions:

With a diagnosis of Nystagmus, it is important to consider whether there is an underlying condition causing Nystagmus. These are other medical conditions that may possibly cause Nystagmus. For general information on this form of misdiagnosis, see Underlying Condition Misdiagnosis or Overview of Misdiagnosis.