Fever, and Psychosis

Diseases related with Fever and Psychosis

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

Top matches:

Female restricted epilepsy with intellectual disability is a rare X-linked epilepsy syndrome characterized by febrile or afebrile seizures (mainly tonic-clonic, but also absence, myoclonic, and atonic) starting in the first years of life and, in most cases, developmental delay and intellectual disability of variable severity. Behavioral disturbances (e.g. autistic features, hyperactivity, and aggressiveness) are also frequently associated. This disease affects exclusively females, with male carriers being unaffected, despite an X-linked inheritance.

FEMALE RESTRICTED EPILEPSY WITH INTELLECTUAL DISABILITY Is also known as juberg-hellman syndrome|efmr|epilepsy, female-restricted, with mental retardation

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Scoliosis
  • Ataxia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FEMALE RESTRICTED EPILEPSY WITH INTELLECTUAL DISABILITY

MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1 Is also known as mhp1|fhm

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1

Medium match PORPHYRIA VARIEGATA

Variegate porphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks with or without the presence of cutaneous lesions.

PORPHYRIA VARIEGATA Is also known as variegate porphyria|ppox deficiency|porphyria, south african type|protoporphyrinogen oxidase deficiency|vp

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PORPHYRIA VARIEGATA

Other less relevant matches:

Medium match KUFOR-RAKEB SYNDROME

Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.

KUFOR-RAKEB SYNDROME Is also known as parkinson disease 9, autosomal recessive, juvenile-onset|park9|pallidopyramidal degeneration with supranuclear upgaze paresis and dementia|krppd

Related symptoms:

  • Intellectual disability
  • Seizures
  • Ataxia
  • Nystagmus
  • Spasticity


SOURCES: OMIM ORPHANET MENDELIAN

More info about KUFOR-RAKEB SYNDROME

Medium 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

Medium match CADASIL

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a hereditary cerebrovascular disorder characterized by mid-adult onset of recurrent subcortical ischemic stroke and cognitive impairment progressing to dementia in addition to migraines with aura and mood disturbances seen in about a third of patients.

CADASIL Is also known as dementia, hereditary multi-infarct type|cadasil|cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy|casil|hereditary multi-infarct dementia

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Sensorineural hearing impairment
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about CADASIL

VELOCARDIOFACIAL SYNDROME Is also known as chromosome 22q11.2 deletion syndrome|shprintzen vcf syndrome|vcf syndrome|vcfs

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about VELOCARDIOFACIAL SYNDROME

Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Medium match MELAS

MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.

MELAS Is also known as mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes|melas syndrome|mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MELAS

Sandhoff disease is a progressive neurodegenerative disorder characterized by an accumulation of GM2 gangliosides, particularly in neurons, and is clinically indistinguishable from Tay-Sachs disease (OMIM ).

SANDHOFF DISEASE, INFANTILE FORM Is also known as infantile gm2 gangliosidosis 0 variant|hexosaminidases a and b deficiency|hexosaminidases a and b deficiency, infantile form|gm2-gangliosidosis, type ii

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Ataxia
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about SANDHOFF DISEASE, INFANTILE FORM

Top 5 symptoms//phenotypes associated to Fever and Psychosis

Symptoms // Phenotype % cases
Seizures Very Common - Between 80% and 100% cases
Intellectual disability Very Common - Between 80% and 100% cases
Ataxia Common - Between 50% and 80% cases
Cognitive impairment Common - Between 50% and 80% cases
Confusion Common - Between 50% and 80% cases

Other less frequent symptoms

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

Common Symptoms - More than 50% cases

Hallucinations

Uncommon Symptoms - Between 30% and 50% cases

Nystagmus

Common Symptoms - More than 50% cases

Hyperreflexia

Uncommon Symptoms - Between 30% and 50% cases

Global developmental delay Short stature Pain Tremor Anxiety Dementia Psychotic episodes Peripheral neuropathy Hearing impairment Depressivity Dysarthria Hypertension Visual hallucinations Hemiplegia Mental deterioration Muscular hypotonia Migraine Cerebral cortical atrophy Headache Gait disturbance Hypertonia Vomiting Muscle weakness Generalized hypotonia EEG abnormality Spasticity Delayed speech and language development Cutaneous photosensitivity Emotional lability Diarrhea Dysmetria Nausea Amenorrhea Attention deficit hyperactivity disorder Behavioral abnormality Myopathy Hypopigmented skin patches Autism Delusions Encephalopathy Hyperactivity Developmental regression Vertigo Dysphagia Dystonia Photophobia Babinski sign Intellectual disability, severe Abnormality of the eye Scoliosis Pulmonary embolism Apathy Aggressive behavior Stroke Urinary incontinence Coma Specific learning disability Motor delay Cerebellar atrophy Gait ataxia Hemiparesis Abnormality of the pinna Growth delay Generalized tonic-clonic seizures

Rare Symptoms - Less than 30% cases

Narrow palpebral fissure Amaurosis fugax Malabsorption Anemia Cataract Gastroesophageal reflux Personality changes Hydrocephalus Ptosis Primary amenorrhea Abnormal facial shape Strabismus Stroke-like episode Pseudobulbar paralysis Upper motor neuron dysfunction Supranuclear gaze palsy Failure to thrive Feeding difficulties Microcephaly Hypothyroidism Mask-like facies Obesity Ventriculomegaly Congestive heart failure Abnormality of the dentition Schizophrenia High palate Nasal speech Visual loss Truncal ataxia Peripheral demyelination Memory impairment Inflammation of the large intestine Blindness Bicuspid aortic valve Basal ganglia calcification Impaired pain sensation Abnormality of visual evoked potentials Congenital cataract Hypoglycemia Elevated serum creatine phosphokinase Transient ischemic attack Seborrheic dermatitis Purpura Cerebral ischemia Visual impairment Sensorineural hearing impairment Skeletal muscle atrophy Hepatomegaly Anal atresia Vitiligo Hypoparathyroidism Short neck Kyphosis Chronic diarrhea Aphasia Adrenal insufficiency Abnormality of extrapyramidal motor function Abnormal blistering of the skin Abdominal pain Pruritus Paralysis Nausea and vomiting Hypogonadotrophic hypogonadism Hypopigmentation of the skin Tetraplegia Hypertrichosis Clinodactyly Respiratory tract infection Bradykinesia Chronic kidney disease Insomnia Motor polyneuropathy Weight loss Fatigue Intellectual disability, mild Constipation Carious teeth Myoclonus Polymicrogyria Hip dysplasia Generalized myoclonic seizures Abnormality of the cardiovascular system Febrile seizures Status epilepticus Type II diabetes mellitus Bruxism Edema Neoplasm Paresthesia Abnormal cerebellum morphology Agitation Dysphasia Drowsiness Migraine with aura Auditory hallucinations Delayed puberty Cerebral atrophy Apnea Diabetes mellitus Postural instability Abnormality of eye movement Lethargy Recurrent respiratory infections Hyporeflexia Neurodegeneration Hypogonadism Osteoporosis Brain atrophy Chorea Muscle cramps Hypertrophic cardiomyopathy Feeding difficulties in infancy Insulin resistance Large hands Sudden cardiac death Polyphagia Narrow nasal bridge Sensory impairment Erythema Myeloid leukemia Bradycardia Proteinuria Striae distensae Radial deviation of finger Myalgia Hypopigmentation of hair Increased serum lactate Jaundice Protruding ear Abnormality of the liver External genital hypoplasia Oligohydramnios Albinism Nephropathy Glucose intolerance Hirsutism Lactic acidosis Narrow forehead Peripheral axonal neuropathy Skeletal muscle hypertrophy Decreased fetal movement Polyneuropathy Ichthyosis Ophthalmoplegia Arthrogryposis multiplex congenita Decreased muscle mass Clumsiness Acidosis Neurological speech impairment Truncal obesity Nyctalopia Dilated cardiomyopathy Rod-cone dystrophy Dyspnea Hypoplastic labia minora Infantile muscular hypotonia Poor suck Hypertelorism Acromicria Poor gross motor coordination Almond-shaped palpebral fissure Abdominal obesity Hypopnea Poor fine motor coordination Narrow palm Central adrenal insufficiency Scrotal hypoplasia Temperature instability Failure to thrive in infancy Precocious puberty Triangular mouth Disseminated intravascular coagulation Erysipelas Anteverted ears Frontal upsweep of hair Clitoral hypoplasia Hyperinsulinemia Cor pulmonale Sleep apnea Cerebellar hypoplasia Overweight Delayed skeletal maturation Hypoventilation Areflexia Arrhythmia Iris hypopigmentation Aortic valve stenosis Abnormality of lipid metabolism Renal insufficiency Increased body weight Central hypotonia Oligomenorrhea Optic atrophy Cardiomyopathy Respiratory distress Acrocyanosis Hypoplasia of the fovea Chromosome breakage Ocular albinism Hypothermia Generalized hypopigmentation Spontaneous abortion Respiratory insufficiency Cerebral calcification Vestibular dysfunction Pigmentary retinopathy Dysesthesia Abnormal macular morphology Hemeralopia Crohn's disease Abnormality of the cerebellar vermis Tubulointerstitial abnormality Renal Fanconi syndrome Abnormal nerve conduction velocity Gastroparesis Spontaneous hematomas Leber optic atrophy Persistence of primary teeth Writer's cramp Muscle fiber atrophy Psychomotor deterioration Episodic vomiting Paronychia Anterior hypopituitarism Renal tubular dysfunction Tubulointerstitial nephritis Increased CSF lactate Wolff-Parkinson-White syndrome Reduced consciousness/confusion Gait imbalance Left ventricular failure Abnormality of the renal tubule Speech apraxia Retinal pigment epithelial atrophy Abnormality of peripheral nerve conduction Proximal tubulopathy Ileus Hemianopia Spotty hypopigmentation Abnormal mitochondrial morphology Facial diplegia Hepatosplenomegaly Abnormality of glycosphingolipid metabolism Cherry red spot of the macula Progressive psychomotor deterioration Motor deterioration Megalencephaly Episodic abdominal pain Orthostatic hypotension Impotence Fasciculations Hypohidrosis Progressive neurologic deterioration Cardiomegaly Progressive cerebellar ataxia Macroglossia Coarse facial features Edema of the dorsum of hands Homonymous hemianopia Cochlear malformation Progressive night blindness Cochlear degeneration Abnormal mitochondrial shape Paralytic ileus Abnormal cochlea morphology Abnormality of acid-base homeostasis Hyperhidrosis Episodic quadriplegia Bilateral intracranial calcifications Morphological abnormality of the vestibule of the inner ear Morphological abnormality of the inner ear Prominent ear helix Macrocephaly Aortic dissection Cardiorespiratory arrest Generalized-onset seizure Type I diabetes mellitus Cachexia Atrioventricular block Growth abnormality Easy fatigability Hyperkinesis Goiter Mutism Ischemic stroke Ragged-red muscle fibers Reduced tendon reflexes External ophthalmoplegia Pancreatitis Macular degeneration Exercise intolerance Generalized hirsutism Hypercalciuria Decreased body weight Bilateral sensorineural hearing impairment Nephrotic syndrome Pulmonary arterial hypertension Ventricular hypertrophy Atrial fibrillation Involuntary movements Left ventricular hypertrophy EMG abnormality Anorexia Gingival overgrowth Abnormality of retinal pigmentation Cerebral visual impairment Clonus Cardiac arrest Decreased nerve conduction velocity Bilateral ptosis Posterior subcapsular cataract Distal arthrogryposis Glomerulopathy Hyperthyroidism Rhabdomyolysis Thyroiditis Abnormality of immune system physiology Primary adrenal insufficiency Atopic dermatitis Vertebral fusion Hashimoto thyroiditis Neonatal hypoglycemia Xerostomia Heart block Mitochondrial myopathy Progressive external ophthalmoplegia Progressive sensorineural hearing impairment Multiple lipomas Aortic aneurysm Hemiplegia/hemiparesis Abnormality of mitochondrial metabolism Hyponatremia Ophthalmoparesis Intestinal obstruction Aplasia/Hypoplasia of the cerebellum Bifid scrotum Focal segmental glomerulosclerosis Prolonged QT interval Abnormality of neuronal migration Overlapping toe Bundle branch block Esotropia Hyperkalemia Visual field defect Growth hormone deficiency Bipolar affective disorder Gastrointestinal hemorrhage Aminoaciduria Glabellar reflex Hyperphenylalaninemia Neural tube defect Glossitis Mood changes Abnormal urinary color Methylmalonic aciduria Episodic ataxia Gingivitis Irregular hyperpigmentation Encephalitis Abnormality of vision Diplopia Neutral hyperaminoaciduria Inflammatory abnormality of the skin Aciduria Hepatic steatosis Cirrhosis Unsteady gait Skin rash Lingual dystonia Eyelid apraxia Hyperactive patellar reflex Upgaze palsy Difficulty in tongue movements Cerebellar cortical atrophy Grasp reflex Facial palsy Stooped posture Scotoma Subcortical dementia Retinal arteriolar tortuosity Focal sensory seizure Diffuse leukoencephalopathy Subcutaneous hemorrhage Mania Perseveration Abnormality of nervous system morphology Varicose veins Optic neuropathy Amyloidosis Bulbar palsy Cerebral hemorrhage Pallor Abnormal electroretinogram Leukoencephalopathy Cranial nerve paralysis Shock Atherosclerosis Spastic tetraparesis Recurrent pneumonia Myocardial infarction Tetraparesis Abnormality of the skin Sensory neuropathy Inability to walk Lower limb muscle weakness Abnormality of higher mental function Leg muscle stiffness Recurrent subcortical infarcts Scarring Difficulty walking Porphyrinuria Premature adrenarche Dark urine Neoplasm of the liver Hepatocellular carcinoma Restlessness Fragile skin Milia Aspiration Thin skin Tachycardia Abnormality of the kidney Abnormal pyramidal sign Carcinoma Abnormality of the skeletal system Transient unilateral blurring of vision Dyscalculia Retinal degeneration Intermittent hyperventilation Hemiclonic seizures Hyperventilation Atonic seizures Absence seizures Epileptic encephalopathy Focal-onset seizure Autistic behavior Rigidity Spastic paraplegia Oculogyric crisis Blepharospasm Hyperreflexia in upper limbs Vertical supranuclear gaze palsy Anarthria Vacuolated lymphocytes Cogwheel rigidity Parkinsonism with favorable response to dopaminergic medication Hyposmia Short attention span Diffuse cerebral atrophy Hypomimic face Slow saccadic eye movements Abnormality of finger Lower limb hyperreflexia Abnormality of the foot Hypokinesia Bowel incontinence Global brain atrophy Akinesia Anosmia Torticollis Paraparesis Intention tremor Parkinsonism Generalized muscle weakness Dyskinesia Distal sensory impairment Paraplegia Abulia Nonarteritic anterior ischemic optic neuropathy Full cheeks Velopharyngeal insufficiency Micrognathia Unilateral primary pulmonary dysgenesis Unilateral lung agenesis Sacral meningocele Right aortic arch with mirror image branching Congenital conductive hearing impairment Perineal fistula Vascular ring Central nervous system degeneration Arteria lusoria Aplasia of the thymus Conotruncal defect Giant platelets Depressed nasal bridge Retinal vascular tortuosity Paranoia Duodenal stenosis Impaired T cell function Right aortic arch Mood swings Platybasia Perimembranous ventricular septal defect Interrupted aortic arch Graves disease Aplasia of the uterus Juvenile rheumatoid arthritis Pulmonary artery atresia Cryptorchidism Epicanthus Echolalia Leukemia Sepsis Sleep disturbance Tapered finger Short foot Small hand Downturned corners of mouth Short palm Arachnodactyly Infertility Genu valgum Hypermetropia Dolichocephaly Abnormality of the nervous system Myopia Neonatal hypotonia Thin upper lip vermilion Osteopenia Narrow mouth Micropenis Respiratory failure Upslanted palpebral fissure Prominent forehead Dilatation Syndactyly Short nose Talipes equinovarus Intrauterine growth retardation Abnormality of the endocrine system Myelomeningocele Scintillating scotoma Inguinal hernia Vesicoureteral reflux Bifid uvula Hemolytic anemia Bulbous nose Pulmonic stenosis Autoimmunity Blepharophimosis Arthritis Conductive hearing impairment Umbilical hernia Retrognathia Posteriorly rotated ears Abnormal heart morphology Renal agenesis Patent ductus arteriosus Hypospadias Hernia Thrombocytopenia Absent speech Abnormality of cardiovascular system morphology Recurrent infections Immunodeficiency Atrial septal defect Hypoplasia of the corpus callosum Ventricular septal defect Cleft palate Subdural hemorrhage Underdeveloped nasal alae Tetralogy of Fallot Truncus arteriosus Acne Pierre-Robin sequence Meningocele Hearing abnormality Posterior embryotoxon Anal stenosis Autoimmune thrombocytopenia Submucous cleft hard palate Axonal loss Autoimmune hemolytic anemia Abnormality of the ear Myopathic facies Hypoplasia of the brainstem Unilateral renal agenesis Low posterior hairline Obsessive-compulsive behavior Psoriasiform dermatitis Rheumatoid arthritis Dysdiadochokinesis Cholelithiasis Abnormality of the hand Arnold-Chiari malformation Holoprosencephaly Multicystic kidney dysplasia Hypocalcemia Spina bifida Renal dysplasia Open mouth Impaired thermal sensitivity


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Motor delay and Pneumonia, related diseases and genetic alterations Congestive heart failure and Hypoglycemia, related diseases and genetic alterations