Visual impairment, and Hypotension
Diseases related with Visual impairment and Hypotension
In the following list you will find some of the most common rare diseases related to Visual impairment and Hypotension that can help you solving undiagnosed cases.
Top matches:
Low match PITUITARY APOPLEXY
The sudden loss of blood supply to the PITUITARY GLAND, leading to tissue NECROSIS and loss of function (PANHYPOPITUITARISM). The most common cause is hemorrhage or INFARCTION of a PITUITARY ADENOMA. It can also result from acute hemorrhage into SELLA TURCICA due to HEAD TRAUMA; INTRACRANIAL HYPERTENSION; or other acute effects of central nervous system hemorrhage. Clinical signs include severe HEADACHE; HYPOTENSION; bilateral visual disturbances; UNCONSCIOUSNESS; and COMA.
Related symptoms:
- Ptosis
- Hypertension
- Fever
- Fatigue
- Headache
SOURCES: MESH ORPHANET MENDELIAN
More info about PITUITARY APOPLEXYLow match PROLACTINOMA
Prolactinoma is a usually benign neoplasm of the pituitary gland that results in hyperprolactinemia. The most common clinical manifestations are amenorrhea and infertility in women; and impotence, decreased libido and infertility in men.
PROLACTINOMA Is also known as pituitary lactotrophic adenoma|prloma|prl-secreting pituitary adenoma|prolactin-secreting pituitary adenoma|lactotroph adenoma|prolactinoma, familial
Related symptoms:
- Seizures
- Neoplasm
- Ptosis
- Fatigue
- Blindness
SOURCES: ORPHANET OMIM MENDELIAN
More info about PROLACTINOMAAdult-onset autosomal dominant leukodystrophy (ADLD) is a rare slowly progressive neurological disorder involving centralnervous systemdemyelination, leading to autonomic dysfunction,ataxia and mild cognitive impairment.
ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHY Is also known as adld|adult-onset autosomal dominant demyelinating leukodystrophy|pelizaeus-merzbacher disease, autosomal dominant or late-onset type, formerly
Related symptoms:
- Global developmental delay
- Hearing impairment
- Ataxia
- Nystagmus
- Spasticity
SOURCES: MESH ORPHANET OMIM MENDELIAN
More info about ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHYOther less relevant matches:
Low match METACHROMATIC LEUKODYSTROPHY, ADULT FORM
METACHROMATIC LEUKODYSTROPHY, ADULT FORM Is also known as arylsulfatase a deficiency, adult form|mld, adult form
Related symptoms:
- Seizures
- Generalized hypotonia
- Muscle weakness
- Spasticity
- Dysarthria
More info about METACHROMATIC LEUKODYSTROPHY, ADULT FORM
Low match TSH-SECRETING PITUITARY ADENOMA
A rare adenoma of the anterior lobe of the pituitary gland that produces thyrotropin. It is usually associated with goiter and hyperthyroidism.
TSH-SECRETING PITUITARY ADENOMA Is also known as thyrotroph adenoma|pituitary thyrotrophic adenoma|thyroid stimulating hormone-secreting pituitary adenoma|tsh-oma
Related symptoms:
- Seizures
- Ptosis
- Hypertension
- Tremor
- Fatigue
More info about TSH-SECRETING PITUITARY ADENOMA
Low match CRANIOPHARYNGIOMA
Craniopharyngiomas are benign slow growing tumours that are located within the sellar and parasellar regions of the central nervous system.
Related symptoms:
- Intellectual disability
- Seizures
- Global developmental delay
- Hearing impairment
- Growth delay
More info about CRANIOPHARYNGIOMA
Low match ATTRV30M AMYLOIDOSIS
Familial amyloid polyneuropathy (FAP) or transthyretin (TTR) amyloid polyneuropathy is a progressive sensorimotor and autonomic neuropathy of adulthood onset. Weight loss and cardiac involvement are frequent; ocular or renal complications may also occur.
ATTRV30M AMYLOIDOSIS Is also known as familial amyloid polyneuropathy type i|ttr amyloid neuropathy|attrv30m-related amyloidosis|hereditary amyloidosis, transthyretin-related|transthyretin amyloid polyneuropathy|familial amyloid polyneuropathy, portuguese-swedish-japanese type|fap|amyloid pol
Related symptoms:
- Seizures
- Hearing impairment
- Ataxia
- Nystagmus
- Sensorineural hearing impairment
SOURCES: OMIM ORPHANET MENDELIAN
More info about ATTRV30M AMYLOIDOSISLow match DOPAMINE BETA-HYDROXYLASE DEFICIENCY
Dopamine beta-hydroxylase deficiency is an extremely rare genetic metabolic disorder characterized by autonomic dysregulation leading mainly to orthostatic hypotension.
DOPAMINE BETA-HYDROXYLASE DEFICIENCY Is also known as norepinephrine deficiency|noradrenaline deficiency
Related symptoms:
- Seizures
- Generalized hypotonia
- Muscular hypotonia
- Pain
- Ptosis
SOURCES: ORPHANET MESH OMIM MENDELIAN
More info about DOPAMINE BETA-HYDROXYLASE DEFICIENCYLow match SANDHOFF DISEASE, INFANTILE FORM
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 FORMLow match TRIPLE A SYNDROME
Triple A syndrome is a very rare multisystem disease characterized by adrenal insufficiency with isolated glucocorticoid deficiency, achalasia, alacrima, autonomic dysfunction and neurodegeneration.
TRIPLE A SYNDROME Is also known as glucocorticoid deficiency and achalasia|quaternary a syndrome|addisonian-achalasia syndrome|achalasia-addisonianism-alacrima syndrome|alacrima-achalasia-adrenal insufficiency neurologic disorder|2a syndrome|3a syndrome|adrenal insufficiency-achalasia-alac
Related symptoms:
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Microcephaly
SOURCES: ORPHANET OMIM MENDELIAN
More info about TRIPLE A SYNDROMETop 5 symptoms//phenotypes associated to Visual impairment and Hypotension
| Symptoms // Phenotype | % cases |
|---|---|
| Seizures | Common - Between 50% and 80% cases |
| Impotence | Common - Between 50% and 80% cases |
| Vomiting | Common - Between 50% and 80% cases |
| Orthostatic hypotension | Common - Between 50% and 80% cases |
| Peripheral neuropathy | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms
Patients with Visual impairment and Hypotension. may also develop some of the following symptoms:
Uncommon Symptoms - Between 30% and 50% cases
Dysarthria Hypoglycemia Fatigue Headache Bitemporal hemianopia Ataxia Hearing impairment Babinski sign Urinary incontinence Abnormal autonomic nervous system physiology Muscle weakness Dementia Vertigo Ptosis Nausea and vomiting Delayed puberty Sudden loss of visual acuity Hypogonadism Pallor Cranial nerve paralysis Hypogonadotrophic hypogonadism Growth hormone excess Orthostatic hypotension due to autonomic dysfunction Diplopia Central adrenal insufficiency Blindness Arrhythmia Constipation Coma Global developmental delay Confusion Spasticity Hyperreflexia Tremor Optic atrophy Prolactin excess Hypertension Hyperhidrosis Weight loss Intellectual disability Pituitary hypothyroidism Adrenocorticotropic hormone deficiencyRare Symptoms - Less than 30% cases
Paraplegia Hypohidrosis Hemiparesis Progressive neurologic deterioration Peripheral demyelination Gliosis Progressive cerebellar ataxia Pain Cerebral cortical atrophy Amyloidosis Depressivity Cardiomegaly Dysphagia Enlarged pituitary gland Sensorineural hearing impairment Abnormal visual field test Congestive heart failure Leukodystrophy Progressive psychomotor deterioration Muscular hypotonia Emotional lability Abnormality of the nervous system Abnormality of visual evoked potentials Bilateral sensorineural hearing impairment Increased CSF protein Hydrocephalus Developmental regression Hyporeflexia Peripheral axonal neuropathy Hallucinations Generalized hypotonia Skeletal muscle atrophy Multiple myeloma Neurodegeneration Abnormality of glycosphingolipid metabolism Bowel incontinence Spastic tetraparesis Spastic paraparesis Paraparesis Polyneuropathy Tetraparesis Hypopituitarism Amenorrhea Osteopenia Decreased circulating ACTH level Decreased female libido Secondary growth hormone deficiency Decreased fertility in females Central diabetes insipidus Excessive daytime somnolence Progressive visual loss Abnormality of the menstrual cycle Nystagmus Blurred vision Oculomotor nerve palsy Gynecomastia Hemianopia Easy fatigability Male hypogonadism Pituitary adenoma Menstrual irregularities Female hypogonadism Adrenocorticotropin deficient adrenal insufficiency Osteoporosis Fourth cranial nerve palsy Heteronymous hemianopia Abnormality of hair density Internal ophthalmoplegia Decreased fertility in males Reduced visual acuity Fever Neoplasm Cranial nerve VI palsy Erectile abnormalities Galactorrhea Abnormality of the pituitary gland Anterior hypopituitarism Decreased number of peripheral myelinated nerve fibers Achalasia Decreased circulating cortisol level Rheumatoid arthritis Restrictive cardiomyopathy Axonal degeneration Primary adrenal insufficiency Stroke-like episode Aphasia Syringomyelia Constrictive median neuropathy Myelopathy Malnutrition Cerebral hemorrhage Motor axonal neuropathy Tachycardia Cachexia Arthritis Craniopharyngioma Intracranial cystic lesion Neoplasm of the anterior pituitary Abnormal hypothalamus morphology Abnormality of the nasal bone Abnormality of the frontal bone Abnormality of the hypothenar eminence Cardiomyopathy Diarrhea Renal insufficiency Areflexia Facial palsy Atrioventricular block Abnormality of the calf musculature Malabsorption Paresthesia Anisocoria Plantar hyperkeratosis Nephropathy Sensory ataxia Alacrima Decreased circulating aldosterone level Migraine Neuronal loss in central nervous system Vasculitis Abnormal renal physiology Syncope Urinary retention Slow decrease in visual acuity Psychosis Chronic diarrhea Fasciculations Hemiplegia Episodic abdominal pain Megalencephaly Supranuclear gaze palsy Parkinsonism Motor deterioration Palmoplantar keratoderma Upper motor neuron dysfunction Paralysis Cherry red spot of the macula Impaired thermal sensitivity Short stature Microcephaly Cognitive impairment Feeding difficulties Iris coloboma Respiratory insufficiency Dilatation Pes cavus Hyperkeratosis Macroglossia Respiratory tract infection Psychomotor deterioration Dehydration Vitreous floaters Generalized hyperpigmentation Cardiac amyloidosis Ectopic kidney Adrenal insufficiency Amyloid deposition in the vitreous humor Oral-pharyngeal dysphagia Palmoplantar hyperkeratosis High palate Myalgia Epiphora Hepatosplenomegaly Neonatal hypoglycemia Hypothermia Recurrent hypoglycemia Hyperpigmentation of the skin Nocturia Intermittent hypothermia Retrograde ejaculation Hepatomegaly Macrocephaly Recurrent respiratory infections Coarse facial features Progressive visual field defects Progressive gait ataxia Cerebral ischemia Heat intolerance Limb muscle weakness Lower limb muscle weakness Abnormal cerebellum morphology Limb ataxia Leukoencephalopathy Abnormality of the urinary system Apathy Personality changes Urinary urgency Progressive spasticity Action tremor Corpus callosum atrophy Abnormal pyramidal sign Neurogenic bladder Pseudobulbar paralysis Atrophy of the spinal cord Diffuse white matter abnormalities Diffuse leukoencephalopathy Autonomic bladder dysfunction Autonomic erectile dysfunction Cervical spinal cord atrophy Dilatation of the bladder Decreased sweating due to autonomic dysfunction Symmetric peripheral demyelination Abnormality of the cerebral white matter Mental deterioration Difficulty walking Abnormal kinetic perimetry test Photophobia Growth hormone deficiency Hypergonadotropic hypogonadism Hyponatremia Increased circulating cortisol level Oligomenorrhea Normochromic anemia Abnormality of the cerebrospinal fluid Mydriasis Prolactin deficiency Trigeminal neuralgia Thunderclap headache Rigidity Abnormal caudate nucleus morphology Abnormal static automated perimetry test Neoplasm of the endocrine system Pituitary prolactin cell adenoma Dyspareunia Prolactinoma Gait disturbance Hypertonia Intellectual disability, mild Encephalopathy Visual loss Dystonia Abdominal distention Papilledema Lethargy Increased thyroid-stimulating hormone level Periodic hypokalemic paresis Euthyroid hyperthyroxinemia Thyroid crisis Growth delay Behavioral abnormality Recurrent infections Obesity Hypothyroidism Anxiety Postnatal growth retardation Nausea Increased circulating gonadotropin level Sleep disturbance Cerebral calcification Type II diabetes mellitus Myocardial infarction Increased body weight Sleep apnea Increased intracranial pressure Increased susceptibility to fractures Diabetes insipidus Polyphagia Proportionate short stature Supraventricular arrhythmia Hyperthyroidism Chorea Cholecystitis Memory impairment Intention tremor Clumsiness Frequent falls Schizophrenia Decreased nerve conduction velocity Loss of speech Delusions Bulbar signs Short attention span Vegetative state Progressive peripheral neuropathy Pericardial effusion EMG: chronic denervation signs Progressive spastic quadriplegia Decerebrate rigidity Abnormal social behavior Punctate periventricular T2 hyperintense foci Abnormality of proteoglycan metabolism Neoplasm of the gallbladder Infertility Palpitations Ventricular arrhythmia Goiter Hypokalemia Adrenocorticotropin receptor defectIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Arthritis and Waddling gait, related diseases and genetic alterations Myopia and Amenorrhea, related diseases and genetic alterations Motor delay and Agenesis of corpus callosum, related diseases and genetic alterations