Fever, and Vertigo

Diseases related with Fever and Vertigo

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

Top matches:

MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 Is also known as mhp2

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM MENDELIAN

More info about CYCLIC VOMITING SYNDROME; CVS

Neurohypophyseal diabetes insipidus is an autosomal dominant disorder of free water conservation characterized by childhood onset of polyuria and polydipsia. Affected individuals are apparently normal at birth, but characteristically develop symptoms of vasopression deficiency during childhood (summary by Wahlstrom et al., 2004).

DIABETES INSIPIDUS, NEUROHYPOPHYSEAL Is also known as diabetes insipidus, cranial type|diabetes insipidus, primary central|cdi

Related symptoms:

  • Intellectual disability
  • Seizures
  • Growth delay
  • Hypertelorism
  • Neoplasm


SOURCES: OMIM MENDELIAN

More info about DIABETES INSIPIDUS, NEUROHYPOPHYSEAL

Other less relevant matches:

High match LASSA FEVER

Lassa fever (LF) is a potentially severe viral hemorrhagic disease caused by Lassa virus and characterized by initial fever and malaise followed by gastrointestinal symptoms and, in severe cases, bleeding, shock and multi-organ system failure.

LASSA FEVER Is also known as lassa hemorrhagic fever|lf

Related symptoms:

  • Seizures
  • Hearing impairment
  • Fever
  • Fatigue
  • Diarrhea


SOURCES: MESH ORPHANET MENDELIAN

More info about LASSA FEVER

Episodic ataxia is a genetically heterogeneous neurologic condition characterized by spells of incoordination and imbalance, often associated with progressive ataxia. Episodic ataxia type 2 is the most common form of EA (Jen et al., 2007).For a discussion of genetic heterogeneity of episodic ataxia, see EA1 (OMIM ).

EPISODIC ATAXIA, TYPE 2; EA2 Is also known as cerebellopathy, hereditary paroxysmal|ataxia, familial paroxysmal|capa|acetazolamide-responsive hereditary paroxysmal cerebellar ataxia|apca|cerebellar ataxia, paroxysmal, acetazolamide-responsive|ataxia, episodic, with nystagmus|episodic ataxia, nystagmu

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about EPISODIC ATAXIA, TYPE 2; EA2

High match HARTNUP DISEASE

Hartnup disease is a rare metabolic disorder belonging to the neutral aminoacidurias and characterized by abnormal renal and gastrointestinal transport of neutral amino acids (tryptophan, alanine, asparagine, glutamine, histidine, isoleucine, leucine, phenylalanine, serine, threonine, tyrosine and valine).

HARTNUP DISEASE Is also known as aminoaciduria, hartnup type|hartnup disease|hartnup disorder

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about HARTNUP DISEASE

Gitelman syndrome is an autosomal recessive renal tubular salt-wasting disorder characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. It is the most common renal tubular disorder among Caucasians (prevalence of 1 in 40,000). Most patients have onset of symptoms as adults, but some can present in childhood. Clinical features include transient periods of muscle weakness and tetany, abdominal pains, and chondrocalcinosis (summary by Glaudemans et al., 2012). Gitelman syndrome is sometimes referred to as a mild variant of classic Bartter syndrome (OMIM ).For a discussion of genetic heterogeneity of Bartter syndrome, see {607364}.

GITELMAN SYNDROME; GTLMNS Is also known as hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria|potassium and magnesium depletion

Related symptoms:

  • Seizures
  • Short stature
  • Generalized hypotonia
  • Ataxia
  • Growth delay


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about GITELMAN SYNDROME; GTLMNS

Deafness - lymphedema - leukemia is a very rare, serious syndromic genetic disorder characterized by primary lymphedema, immunodeficiency, and hematological disorders.

DEAFNESS-LYMPHEDEMA-LEUKEMIA SYNDROME Is also known as emberger syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Sensorineural hearing impairment
  • Anemia
  • Epicanthus


SOURCES: OMIM ORPHANET MENDELIAN

More info about DEAFNESS-LYMPHEDEMA-LEUKEMIA SYNDROME

Waldenström macroglobulinemia (WM) is an indolent B-cell lymphoproliferative disorder characterized by the accumulation of monoclonal cells in the bone marrow and peripheral lymphoid tissues, and associated with the production of serum immunoglobulin M (IgM) monoclonal protein.

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Neoplasm
  • Anemia
  • Peripheral neuropathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about WALDENSTRÖM MACROGLOBULINEMIA

Tumor necrosis factor receptor 1 associated periodic syndrome (TRAPS) is a periodic fever syndrome, characterized by recurrent fever, arthralgia, myalgia and tender skin lesions lasting for 1 to 3 weeks, associated with skin, joint, ocular and serosal inflammation and complicated by secondary amyloidosis (see this term).

TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME Is also known as tnf receptor 1-associated periodic syndrome|fpf|traps syndrome|hibernian fever, familial|familial hibernian fever|fhf|tnf receptor-associated periodic syndrome|tumor necrosis factor receptor-associated periodic syndrome|traps

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Fever
  • Edema


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME

Top 5 symptoms//phenotypes associated to Fever and Vertigo

Symptoms // Phenotype % cases
Migraine Common - Between 50% and 80% cases
Fatigue Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Headache Common - Between 50% and 80% cases
Vomiting Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Fever and Vertigo. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Ataxia

Uncommon Symptoms - Between 30% and 50% cases

Diarrhea Nausea and vomiting Nausea Hearing impairment Intellectual disability Lymphadenopathy Confusion Neoplasm Global developmental delay Paresthesia Generalized hypotonia Abdominal pain Pain Muscle weakness Growth delay Myalgia Episodic ataxia Lethargy Pallor Skin rash Weight loss Diplopia Arthralgia Constipation Dysarthria Depressivity Splenomegaly Nystagmus Anemia Behavioral abnormality Edema Tremor Photophobia

Rare Symptoms - Less than 30% cases

Visual loss Inflammatory abnormality of the skin Episodic fever Thrombocytopenia Erythema Cranial nerve paralysis Pollakisuria Elevated erythrocyte sedimentation rate Enuresis Polyuria Polydipsia Dehydration Hypotension Autoimmunity Periorbital edema Vasculitis Hepatomegaly Leukemia Hypercoagulability Anxiety Short stature Bruising susceptibility Rhabdomyolysis Leukocytosis Cellulitis Generalized muscle weakness Recurrent infections Postural instability Malabsorption Chest pain EEG abnormality Cerebellar atrophy Erysipelas Recurrent pharyngitis Pleural effusion Leukopenia Cirrhosis Conjunctivitis Gastrointestinal hemorrhage Respiratory insufficiency Muscle cramps Nocturia Intention tremor Motor delay Anorexia Gait ataxia Stroke Myopathy Tinnitus Coma Hemiplegia Cognitive impairment Loss of consciousness Blurred vision Muscular hypotonia Strabismus Abnormal cerebellum morphology Neuritis Syndactyly Immunodeficiency Optic neuritis Pleuritis Conjunctival hyperemia Abnormality of neutrophils Chills Recurrent respiratory infections Respiratory failure Scarring Lymphocytosis Neurological speech impairment Hemolytic anemia Hematuria Tapered finger Webbed neck Hypotelorism Pancytopenia Epicanthus Salt craving Abnormality of the sacroiliac joint Alkalosis Ventricular tachycardia Ventricular arrhythmia Hepatic amyloidosis Hyperkinesis Hypokalemia Hypercalciuria Prolonged QT interval Orchitis Hyperventilation Hypomagnesemia Renal salt wasting Chondrocalcinosis Sensorineural hearing impairment Tetany Metabolic alkalosis Increased circulating renin level Periodic paralysis Hypovolemia Hypocalciuria Hypokalemic alkalosis Hypokalemic metabolic alkalosis Renal potassium wasting Hypochloremia Renal magnesium wasting Bone marrow hypocellularity Lymphedema Prolonged bleeding time Intracranial hemorrhage Gingival bleeding Epistaxis Meningitis Peripheral demyelination Hepatic failure Purpura Papule Urticaria Palpitations Cutis marmorata Arthritis Inguinal hernia Pulmonary infiltrates Muscle stiffness Hernia Polyclonal elevation of IgM Cryoglobulinemia Impaired lymphocyte transformation with phytohemagglutinin Raynaud phenomenon Edema of the lower limbs Lymphoproliferative disorder Abnormality of the retinal vasculature Reduced consciousness/confusion Monoclonal immunoglobulin M proteinemia Multifocal epileptiform discharges Normocytic anemia Memory impairment Intestinal obstruction Myelodysplasia Abnormality of the optic nerve Chronic otitis media Elevated C-reactive protein level Retinal hemorrhage Peritonitis Myeloid leukemia Abnormal myocardium morphology Myositis Acute myeloid leukemia Acute leukemia Reticulocytosis Verrucae Uveitis Myeloproliferative disorder Lymphoma Pericarditis Granulocytopenia Amyloidosis Macronodular cirrhosis Abnormal neutrophil count Peripheral neuropathy Congestive heart failure Renal insufficiency Macule Proptosis Polyneuropathy Hypermelanotic macule Cardiac arrest Gastroesophageal reflux Nephropathy Histiocytosis Abnormality of metabolism/homeostasis Osteoporosis Diabetes mellitus Osteopenia Irritability Dry skin Wide nose Gliosis Syncope Growth hormone deficiency Diabetes insipidus Orthostatic hypotension Central diabetes insipidus Short nose Hypertonic dehydration Abnormality of the anterior pituitary Germinoma Cough Subcutaneous nodule Spontaneous abortion Increased intracranial pressure Palpebral edema Cardiorespiratory arrest Menometrorrhagia Chemosis Scoliosis Skeletal muscle atrophy Long philtrum Hypertelorism Ventriculomegaly Drowsiness Delayed speech and language development Blindness Intellectual disability, mild Intellectual disability, moderate Developmental regression Autistic behavior Dysmetria Apraxia Hemiparesis Aphasia Dysphasia Severe hearing impairment Restlessness Migraine with aura Gastrointestinal dysmotility Phonophobia Borderline personality disorder Migraine without aura Personality disorder Transient unilateral blurring of vision Microcephaly Cardiomyopathy Hyperhidrosis Autism Attention deficit hyperactivity disorder Abnormal autonomic nervous system physiology Exercise intolerance Abnormality of mitochondrial metabolism Optic atrophy Hypoplasia of the corpus callosum Tachycardia Bruxism Psychosis Cutaneous photosensitivity Chronic diarrhea Hallucinations Aminoaciduria Hypopigmented skin patches Abnormality of vision Encephalitis Emotional lability Insomnia Irregular hyperpigmentation Delusions Gingivitis Methylmalonic aciduria Aciduria Abnormal urinary color Mood changes Glossitis Neural tube defect Hyperphenylalaninemia Glabellar reflex Grasp reflex Neutral hyperaminoaciduria Failure to thrive Hypertension Arrhythmia Paralysis Delayed puberty Abnormal blistering of the skin Hepatic steatosis Dystonia Ophthalmoparesis Encephalopathy Rigidity Proximal muscle weakness Facial palsy Apnea Progressive cerebellar ataxia Focal-onset seizure Epileptic encephalopathy Horizontal nystagmus Sleep apnea CNS hypomyelination Incoordination Focal impaired awareness seizure Myotonia Unsteady gait Vestibular dysfunction Gaze-evoked nystagmus Cerebellar vermis atrophy Malignant hyperthermia Saccadic smooth pursuit Downbeat nystagmus Spasticity Ptosis Hyperreflexia Gait disturbance Hydrocephalus Hypertonia Abnormality of the eye Fasciitis


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