Ataxia, and Migraine

Diseases related with Ataxia and Migraine

In the following list you will find some of the most common rare diseases related to Ataxia and Migraine that can help you solving undiagnosed cases.


Top matches:

Medium match INFANTILE CONVULSIONS AND CHOREOATHETOSIS


Infantile Convulsions and paroxysmal ChoreoAthetosis (ICCA) syndrome is a neurological condition characterized by the occurrence of seizures during the first year of life (Benign familial infantile epilepsy ; see this term) and choreoathetotic dyskinetic attacks during childhood or adolescence.

INFANTILE CONVULSIONS AND CHOREOATHETOSIS Is also known as paroxysmal kinesigenic dyskinesia and infantile convulsions|icca syndrome|pkd/ic|infantile convulsions and paroxysmal choreoathetosis, familial|paroxysmal kinesigenic dyskinesia with infantile convulsions

Related symptoms:

  • Seizures
  • Ataxia
  • Dystonia
  • Anxiety
  • Apnea


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about INFANTILE CONVULSIONS AND CHOREOATHETOSIS

Medium match BENIGN PAROXYSMAL TORTICOLLIS OF INFANCY


Benign paroxysmal torticollis of infancy (BPTI) is a rare functional disorder characterised by recurrent episodes of torticollic posturing of the head (inclination or tilting of the head to one side) in healthy children.

Related symptoms:

  • Ataxia
  • Vomiting
  • Irritability
  • Pallor
  • Vertigo


SOURCES: ORPHANET MENDELIAN

More info about BENIGN PAROXYSMAL TORTICOLLIS OF INFANCY

Medium match ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2


Alternating hemiplegia of childhood is a rare syndrome characterized by infantile onset of episodic hemi-or quadriplegia. Most cases are accompanied by dystonic posturing, choreoathetoid movements, abnormal ocular movements, developmental delay, and progressive cognitive impairment (summary by Heinzen et al., 2012).For discussion of genetic heterogeneity of alternating hemiplegia of childhood, see AHC1 (OMIM ).

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2

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Other less relevant matches:

Medium match EPISODIC ATAXIA TYPE 6


Episodic ataxia type 6 (EA6) is an exceedingly rare form of Hereditary episodic ataxia (see this term) with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia.

Related symptoms:

  • Seizures
  • Ataxia
  • Cerebellar atrophy
  • Headache
  • Reduced visual acuity


SOURCES: ORPHANET MENDELIAN

More info about EPISODIC ATAXIA TYPE 6

Medium match PAROXYSMAL DYSTONIC CHOREATHETOSIS WITH EPISODIC ATAXIA AND SPASTICITY


Dystonia-9 is an autosomal dominant neurologic disorder characterized by childhood onset of paroxysmal choreoathetosis and progressive spastic paraplegia. Most show some degree of cognitive impairment. Other variable features may include seizures, migraine headaches, and ataxia (summary by Weber et al., 2011).

PAROXYSMAL DYSTONIC CHOREATHETOSIS WITH EPISODIC ATAXIA AND SPASTICITY Is also known as dyt9|cse choreoathetosis, paroxysmal, with episodic ataxia|episodic choreoathetosis/spasticity|choreoathetosis, kinesigenic, with episodic ataxia and spasticity|choreoathetosis/spasticity, episodic

Related symptoms:

  • Intellectual disability
  • Seizures
  • Ataxia
  • Spasticity
  • Cognitive impairment


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about PAROXYSMAL DYSTONIC CHOREATHETOSIS WITH EPISODIC ATAXIA AND SPASTICITY

Medium match TREMOR, HEREDITARY ESSENTIAL, 1; ETM1


Essential tremor may be the most common human movement disorder. The main feature of essential tremor is postural tremor of the arms, but the head, legs, trunk, voice, jaw, and facial muscles also may be involved. Aggravated by emotions, hunger, fatigue, and temperature extremes, the condition may cause a functional disability or even incapacitation. Autosomal dominant inheritance can be demonstrated in most families (summary by Higgins et al., 1997).Deng et al. (2007) provided a detailed review of the genetics of essential tremor. Genetic Heterogeneity of Essential TremorOther forms of hereditary essential tremor include ETM2 (OMIM ), mapped to chromosome 2p25-p22; ETM3 (OMIM ), mapped to chromosome 6p23; ETM4 (OMIM ), caused by mutation in the FUS gene (OMIM ) on chromosome 16p11; and ETM5 (OMIM ), caused by mutation in the TENM4 gene (OMIM ) on chromosome 11q14.

TREMOR, HEREDITARY ESSENTIAL, 1; ETM1 Is also known as fet1|tremor, familial essential, 1

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Cognitive impairment
  • Dysarthria
  • Fever


SOURCES: OMIM MENDELIAN

More info about TREMOR, HEREDITARY ESSENTIAL, 1; ETM1

Medium match PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT


Women show menstrual cycle-dependent physiologic changes in relation to sex hormone levels. Because ovulation triggers a significant change in the hormonal milieu that is similar to local inflammation, a 0.5 to 1.0 degree Celsius increase in basal body temperature after ovulation is commonly associated with progesterone secretion and is believed to be triggered by the induction of several inflammatory cytokines. Rare menstrual cycle-dependent febrile episodes have been reported, some of which have shown a luteal-phase-dependent pattern (summary by Jiang et al., 2012).

Related symptoms:

  • Ataxia
  • Fever
  • Tremor
  • Myalgia
  • Lower limb muscle weakness


SOURCES: OMIM MENDELIAN

More info about PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT

Medium match FAMILIAL PAROXYSMAL ATAXIA


Episodic ataxia type 2 (EA2) is the most frequent form of Hereditary episodic ataxia (EA; see this term) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.

FAMILIAL PAROXYSMAL ATAXIA Is also known as episodic ataxia type 2

Related symptoms:

  • Intellectual disability
  • Ataxia
  • Nystagmus
  • Dysarthria
  • Behavioral abnormality


SOURCES: ORPHANET MENDELIAN

More info about FAMILIAL PAROXYSMAL ATAXIA

Medium match FAMILIAL OR SPORADIC HEMIPLEGIC MIGRAINE


Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the aura. Hemiplegic migraine has two main forms depending on the familial history: patients with at least one first- or second-degree relative who has aura including motor weakness have familial hemiplegic migraine (FHM); patients without such familial history have sporadic hemiplegic migraine (SHM).

Related symptoms:

  • Seizures
  • Ataxia
  • Nystagmus
  • Sensorineural hearing impairment
  • Blindness


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL OR SPORADIC HEMIPLEGIC MIGRAINE

Medium match ATYPICAL TERATOID RHABDOID TUMOR


Atypical teratoid rhabdoid tumor (ATRT) is a highly malignant central nervous system (CNS) rhabdoid tumor (RT; see this term) found almost exclusively in children.

ATYPICAL TERATOID RHABDOID TUMOR Is also known as atrt

Related symptoms:

  • Seizures
  • Ataxia
  • Muscle weakness
  • Macrocephaly
  • Hydrocephalus


SOURCES: ORPHANET MENDELIAN

More info about ATYPICAL TERATOID RHABDOID TUMOR

Top 5 symptoms//phenotypes associated to Ataxia and Migraine

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Dystonia Uncommon - Between 30% and 50% cases
Dysarthria Uncommon - Between 30% and 50% cases
Headache Uncommon - Between 30% and 50% cases
Hemiplegia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Ataxia and Migraine. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Abnormality of movement Choreoathetosis Diplopia Nausea and vomiting Nystagmus Intellectual disability Cognitive impairment Anxiety Vertigo

Rare Symptoms - Less than 30% cases


Depressivity Tremor Gait disturbance Rigidity Mental deterioration Phonophobia Parkinsonism Hemiparesis Photophobia Hemiplegia/hemiparesis Generalized tonic-clonic seizures Fever Apathy Torticollis Generalized-onset seizure Irritability Vomiting Dyskinesia Paroxysmal dyskinesia Involuntary movements Paroxysmal choreoathetosis Hand tremor Lower limb muscle weakness Myalgia Cerebral palsy Kinetic tremor Head tremor Postural tremor Resting tremor Personality changes Abnormality of extrapyramidal motor function Memory impairment Hypoglycemia Dementia Cerebral atrophy Fatigue Reduced consciousness/confusion Hepatitis Dysphasia Cranial nerve paralysis Neurological speech impairment Migraine with aura Muscle weakness Macrocephaly Pigmentary retinopathy Hearing impairment Nausea Hydrocephalus EEG abnormality Cerebral calcification Blindness Sensorineural hearing impairment Limitation of joint mobility Cerebellar vermis atrophy Tinnitus Behavioral abnormality Recurrent spontaneous abortion Abnormality of retinal pigmentation Increased circulating cortisol level Hyperreflexia Progressive spastic paraparesis Abnormal head movements Status epilepticus Chorea Tetraplegia Abnormality of eye movement Abnormality of the eye Generalized hypotonia Global developmental delay Drowsiness Abnormal autonomic nervous system physiology Pallor Normal interictal EEG Focal seizures, afebril Paroxysmal dystonia Writer's cramp Stereotypy Focal-onset seizure Apnea Tetraparesis Loss of consciousness Morphological abnormality of the pyramidal tract Paresthesia Episodic ataxia Progressive spastic paraplegia Brisk reflexes Spastic paraparesis Paraparesis Clonus Dehydration Postural instability Paraplegia Episodic quadriplegia Spastic paraplegia Abnormal pyramidal sign Babinski sign Spasticity Gaze-evoked nystagmus Slurred speech Reduced visual acuity Cerebellar atrophy Malignant neoplasm of the central nervous system



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