Hypertension, and Sensory neuropathy

Diseases related with Hypertension and Sensory neuropathy

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

Top matches:

Autosomal dominant primary hypomagnesemia with hypocalciuria (ADPHH) is a mild form of familial primary hypomagnesemia (FPH, see this term), characterized by extreme weakness, tetany and convulsions. Secondary disturbances in calcium excretion are observed.

AUTOSOMAL DOMINANT PRIMARY HYPOMAGNESEMIA WITH HYPOCALCIURIA Is also known as isolated renal magnesium wasting|isolated autosomal dominant hypomagnesemia|magnesium wasting, renal|homg2|renal hypomagnesemia type 2|magnesium loss, isolated renal

Related symptoms:

  • Seizures
  • Hypertension
  • Fatigue
  • Renal insufficiency
  • Muscle cramps


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about AUTOSOMAL DOMINANT PRIMARY HYPOMAGNESEMIA WITH HYPOCALCIURIA

Porphyria of doss or deficiency of delta-aminolevulinic acid dehydratase (DALAD) is an extremely rare form of acute hepatic porphyria (see this term) characterized by neuro-visceral attacks without cutaneous manifestations.

PORPHYRIA DUE TO ALA DEHYDRATASE DEFICIENCY Is also known as porphyria due to alad deficiency|doss porphyria|delta-aminolevulinate dehydratase deficiency|alad porphyria|porphyria, alad|porphyria of doss|alad deficiency|porphyria due to delta-aminolevulinate dehydratase deficiency|porphobilinogen synthase deficiency

Related symptoms:

  • Seizures
  • Generalized hypotonia
  • Failure to thrive
  • Muscular hypotonia
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PORPHYRIA DUE TO ALA DEHYDRATASE DEFICIENCY

AMYLOIDOSIS, FAMILIAL VISCERAL Is also known as german type amyloidosis|amyloidosis, systemic nonneuropathic|amyloidosis viii|amyloidosis, familial renal|ostertag type amyloidosis

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Pain
  • Hypertension
  • Peripheral neuropathy


SOURCES: ORPHANET OMIM MENDELIAN

More info about AMYLOIDOSIS, FAMILIAL VISCERAL

Other less relevant matches:

Essential thrombocythemia (ET) is a myeloproliferative neoplasm (MPN, see this term) characterized by a sustained elevation of platelet number (> 450 x 109/L) with a tendency for thrombosis and hemorrhage.

ESSENTIAL THROMBOCYTHEMIA Is also known as thrombocytosis 1|essential thrombocytosis|et

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system
  • Respiratory distress


SOURCES: ORPHANET OMIM MENDELIAN

More info about ESSENTIAL THROMBOCYTHEMIA

Acute intermittent porphyria is the most frequent and the most severe form of the acute hepatic porphyrias (see this term). It is characterized by the occurrence of neuro-visceral attacks without cutaneous manifestations.

ACUTE INTERMITTENT PORPHYRIA Is also known as ups deficiency|porphyria, swedish type|pbgd deficiency|porphobilinogen deaminase deficiency|uroporphyrinogen synthase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Muscle weakness
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ACUTE INTERMITTENT PORPHYRIA

Hereditary coproporphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.

HEREDITARY COPROPORPHYRIA Is also known as cpox deficiency|cpx deficiency|coproporphyrinogen oxidase deficiency|cpo deficiency

Related symptoms:

  • Seizures
  • Muscle weakness
  • Pain
  • Anemia
  • Hypertension


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about HEREDITARY COPROPORPHYRIA

Multiple symmetric lipomatosis (MSL) is a rare subcutaneous tissue disease characterized by growth of symmetric non-encapsulated masses of adipose tissue mostly around the face and neck with variable clinical repercussions (e.g. reduced neck mobility, compression of respiratory structures).

MULTIPLE SYMMETRIC LIPOMATOSIS Is also known as launois-bensaude lipomatosis|familial benign cervical lipomatosis|madelung disease|cephalothoracic lipodystrophy|lipomatosis, familial benign cervical|lipodystrophy, cephalothoracic

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Hypertension
  • Peripheral neuropathy


SOURCES: ORPHANET OMIM MENDELIAN

More info about MULTIPLE SYMMETRIC LIPOMATOSIS

Fragile X-associated tremor/ataxia syndrome (FXTAS) is a rare neurodegenerative disorder characterized by adult-onset progressive intention tremor and gait ataxia.

FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME Is also known as fxtas syndrome

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME

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

Von Hippel-Lindau disease (VHL) is a familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma.

VON HIPPEL-LINDAU DISEASE Is also known as familial cerebelloretinal angiomatosis|von hippel-lindau syndrome|lindau disease|vhl

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Neoplasm
  • Sensorineural hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about VON HIPPEL-LINDAU DISEASE

Top 5 symptoms//phenotypes associated to Hypertension and Sensory neuropathy

Symptoms // Phenotype % cases
Pain Common - Between 50% and 80% cases
Paresthesia Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Tachycardia Uncommon - Between 30% and 50% cases
Abdominal pain Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Hypertension and Sensory neuropathy. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Peripheral neuropathy Diarrhea Arthralgia Anxiety Muscle weakness Vomiting Anemia Nausea and vomiting Hepatosplenomegaly Arrhythmia Hepatomegaly Constipation Hyponatremia Ataxia Psychosis Polyneuropathy Paralysis Respiratory paralysis Neoplasm Gait disturbance Muscle cramps Behavioral abnormality Splenomegaly Nausea Myalgia Nephropathy Depressivity Hypotension Hearing impairment

Rare Symptoms - Less than 30% cases

Abnormality of the cerebral vasculature Global developmental delay Hyperhidrosis Agitation Urinary incontinence Acute episodes of neuropathic symptoms Nystagmus Postural instability Hypothyroidism Confusion Irritability Pollakisuria Red urine Cutaneous photosensitivity Delirium Ileus Insomnia Vertigo Apathy Paraparesis Hallucinations Myocardial infarction Intellectual disability Failure to thrive Hypokalemia Generalized hypotonia Hemolytic anemia Renal magnesium wasting Hypocalciuria Abdominal colic Dysesthesia Elevated urinary delta-aminolevulinic acid Fever Chondrocalcinosis Glaucoma Weight loss Hypomagnesemia Pulmonary embolism Generalized muscle weakness Renal insufficiency Fatigue Abnormality of movement Abnormality of the cerebral white matter Olivopontocerebellar atrophy Astrocytosis Stroke Disinhibition Mental deterioration Vascular neoplasm Aggressive behavior Kinetic tremor Proximal muscle weakness Saccadic smooth pursuit Action tremor Poor fine motor coordination Abnormality of brainstem morphology Abnormal nerve conduction velocity Rigidity Autism Gait ataxia Cerebral cortical atrophy Impaired distal vibration sensation Diffuse cerebellar atrophy Obsessive-compulsive trait Diffuse cerebral atrophy Urinary bladder sphincter dysfunction Abnormal cerebellum morphology Premature ovarian insufficiency Parkinsonism Progressive cerebellar ataxia Brain atrophy Memory impairment Bradykinesia Intention tremor Limb ataxia Horizontal nystagmus Abnormal autonomic nervous system physiology Spastic paraparesis Dysdiadochokinesis Obsessive-compulsive behavior Bipolar affective disorder Distal sensory impairment Postural tremor Mask-like facies Impotence Retrocollis Global brain atrophy Dysmetria Bowel incontinence Abnormality of the thyroid gland Resting tremor Atrophy/Degeneration affecting the brainstem Aplasia/Hypoplasia of the cerebellum Impaired tandem gait Inertia Hypochloremia Renal salt wasting Alkalosis Enuresis Renal cell carcinoma Tetany Metabolic alkalosis Increased circulating renin level Periodic paralysis Hypovolemia Hypokalemic alkalosis Hypokalemic metabolic alkalosis Nocturia Renal potassium wasting Telangiectasia of the skin Episodic fever Salt craving Sensorineural hearing impairment Cataract Hemiplegia/hemiparesis Visual impairment Hydrocephalus Visual loss Abnormality of the kidney Neurological speech impairment Retinal detachment Migraine Multicystic kidney dysplasia Increased intracranial pressure Hyperventilation Rhabdomyolysis Subcortical dementia Cardiac arrest Retinal capillary hemangioma Polycystic kidney dysplasia Short stature Papillary cystadenoma of the epididymis Growth delay Erythema Neuroendocrine neoplasm Abnormality of the lymphatic system Delayed puberty Visceral angiomatosis Dehydration Palpitations Inflammatory abnormality of the skin Pancreatic cysts Prolonged QT interval Pheochromocytoma Ventricular tachycardia Abnormality of the pancreas Abnormality of the retinal vasculature Arteriovenous malformation Ventricular arrhythmia Capillary hemangioma Multiple renal cysts Hyporeflexia Hyperkinesis Hypercalciuria Polydipsia Polyuria Blurred vision Dementia Congenital hemolytic anemia Cerebellar atrophy Impaired platelet aggregation Venous thrombosis Myelodysplasia Leukocytosis Prolonged bleeding time Myeloid leukemia Thrombocytosis Transient ischemic attack Acrocyanosis Gangrene Acute leukemia Arterial thrombosis Abnormal thrombocyte morphology Myeloproliferative disorder Chest pain Amaurosis fugax Abnormality of bone marrow cell morphology Myelofibrosis Bloody diarrhea Abnormal platelet morphology Decreased mean platelet volume Abnormal platelet aggregation Increased megakaryocyte count Intellectual disability, mild Carcinoma Lethargy Stage 5 chronic kidney disease Lymphoma Bruising susceptibility Abdominal distention Cholestasis Chronic fatigue Muscular hypotonia Respiratory insufficiency Hemiparesis Motor axonal neuropathy Wrist drop Cardiomyopathy Edema Proteinuria Skin rash Hematuria Nephrotic syndrome Urticaria Leukemia Amyloidosis Optic neuropathy Papilledema Drusen Restrictive cardiomyopathy Albuminuria Renal amyloidosis Generalized amyloid deposition Abnormality of the skeletal system Respiratory distress Headache Dyspnea Coma Anorexia Dysphagia Macrocytic anemia Abnormality of the liver Abnormality of the skin Insulin resistance Hoarse voice Reduced tendon reflexes Ragged-red muscle fibers Abnormality of mitochondrial metabolism Oral-pharyngeal dysphagia Coronary artery atherosclerosis Axonal degeneration Multiple lipomas Arthropathy Lipoma Diabetes mellitus Oligomenorrhea Gout Hyperlipoproteinemia Alcoholism Decreased LDL cholesterol concentration Neuropathic arthropathy Increased HDL cholesterol concentration Abnormal adipose tissue morphology Cognitive impairment Hyperreflexia Dysarthria Tremor Joint stiffness Pes cavus Hyperlipidemia Jaundice Cranial nerve paralysis Hepatocellular carcinoma Dysuria Urinary retention Diaphragmatic paralysis Abnormal urinary color Psychotic episodes Hypertensive crisis Paralytic ileus Abnormality of metabolism/homeostasis Areflexia Acidosis Elevated hepatic transaminase Babinski sign Pruritus Metabolic acidosis Abnormal blistering of the skin Hypertrichosis Thin skin Hypermelanotic macule Orthostatic hypotension Prolonged neonatal jaundice Fragile skin Visual hallucinations Auditory hallucinations Paranoia Compensated hemolytic anemia Neoplasm of the middle ear


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