Hypertension, and Photophobia

Diseases related with Hypertension and Photophobia

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

Top matches:

Medium 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 APOPLEXY

CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE Is also known as cystinosis, intermediate

Related symptoms:

  • Short stature
  • Failure to thrive
  • Muscle weakness
  • Visual impairment
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE

Senior-Loken syndrome (SLSN) is a very rare autosomal recessive oculo-renal disease characterized by the association of nephronophthisis (NPHP), a chronic kidney disease, with retinal dystrophy.

SENIOR-LOKEN SYNDROME Is also known as renal-retinal syndrome|juvenile nephronophthisis with leber amaurosis|loken-senior syndrome|renal dysplasia-retinal aplasia syndrome|nephronophthisis with retinal dystrophy|slsn|renal dysplasia and retinal aplasia|senior-loken syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about SENIOR-LOKEN SYNDROME

Other less relevant matches:

Alport syndrome is an inherited disorder of the basement membrane, resulting in progressive renal failure due to glomerulonephropathy, variable sensorineural hearing loss, and variable ocular anomalies (review by Kashtan, 1999).Alport syndrome is a genetically heterogeneous disorder, with all forms resulting from mutations in genes encoding type IV collagen, which is a major structural component of the basement membrane. Approximately 85% of cases of Alport syndrome are X-linked and about 15% are autosomal recessive (OMIM ); autosomal dominant inheritance (OMIM ) is rare (Kashtan, 1999).See also benign familial hematuria (BFH ), a phenotypically similar, but milder disorder.Alport syndrome is also a feature of 2 contiguous gene deletion syndromes involving the COL4A5 gene: Alport syndrome and diffuse leiomyomatosis (OMIM ) and Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis (AMME ).

ALPORT SYNDROME, X-LINKED; ATS Is also known as nephropathy and deafness, x-linked

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Sensorineural hearing impairment
  • Cataract
  • Hypertension


SOURCES: ORPHANET OMIM MENDELIAN

More info about ALPORT SYNDROME, X-LINKED; ATS

Medium match BLAU SYNDROME

Blau syndrome (BS) is a rare systemic inflammatory disease characterized by early onset granulomatous arthritis, uveitis and skin rash. BS now refers to both the familial and sporadic (formerly early-onset sarcoidosis) form of the same disease. The proposed term pediatric granulomatous arthritis is currently questioned since it fails to represent the systemic nature of the disease.

Related symptoms:

  • Cataract
  • Anemia
  • Hypertension
  • Fever
  • Splenomegaly


SOURCES: ORPHANET MENDELIAN

More info about BLAU SYNDROME

Xeroderma pigmentosum is an autosomal recessive disorder characterized by sun sensitivity and increased skin sensitivity to UV light, as well as an increased risk of skin cancer associated with a defect in nucleotide excision repair (NER). The XPF form of XP is usually relatively mild compared to other forms. Patients with XPF tend to have later onset of skin cancer. Some patients with XPF may develop neurologic impairment or growth defects, and are then classified as having Cockayne syndrome (summary by Kashiyama et al., 2013).For a general phenotypic description and a discussion of genetic heterogeneity of xeroderma pigmentosa, see XPA (OMIM ), and of Cockayne syndrome, see CSA (OMIM ).

XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF Is also known as xp6|xp, group f|xeroderma pigmentosum vi

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Scoliosis


SOURCES: MESH OMIM MENDELIAN

More info about XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF

Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood with hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and frequently cardiac involvement with arrhythmias and/or cardiomyopathy.

LONG CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY Is also known as lchad deficiency|long-chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency|lchadd

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Failure to thrive


SOURCES: ORPHANET OMIM MENDELIAN

More info about LONG CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY

Medium match SARCOIDOSIS

Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs.

SARCOIDOSIS Is also known as boeck sarcoid|besnier-boeck-schaumann disease|sarcoidosis|boeck's sarcoid

Related symptoms:

  • Seizures
  • Pain
  • Cataract
  • Anemia
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about SARCOIDOSIS

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

Top 5 symptoms//phenotypes associated to Hypertension and Photophobia

Symptoms // Phenotype % cases
Fever Common - Between 50% and 80% cases
Fatigue Common - Between 50% and 80% cases
Renal insufficiency Common - Between 50% and 80% cases
Vomiting Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Short stature Anemia Weight loss Cataract Retinopathy Headache Visual impairment Myopathy Failure to thrive Sensorineural hearing impairment Proteinuria Visual loss Stage 5 chronic kidney disease Nephropathy Seizures Pain Congestive heart failure Global developmental delay Hearing impairment Feeding difficulties Nystagmus Erythema Dyspnea Tubulointerstitial nephritis Nausea Abnormality of the liver Myopia Delayed puberty Nyctalopia Anorexia Hypopigmentation of the skin Papule Edema Hypothyroidism Attention deficit hyperactivity disorder Muscular hypotonia Blindness Pigmentary retinopathy Coma Abnormality of retinal pigmentation Chronic kidney disease Hepatomegaly Peripheral neuropathy Ichthyosis Hypoglycemia Growth delay Ataxia

Rare Symptoms - Less than 30% cases

Facial palsy Glaucoma Generalized hypotonia Splenomegaly Hypoparathyroidism Decreased body weight Abnormal salivary gland morphology Cutaneous photosensitivity Xerostomia Scoliosis Neoplasm Iridocyclitis Erythema nodosum Intrauterine growth retardation Tremor Cerebellar atrophy Cerebral atrophy Hyperactivity Microcephaly Joint swelling Abnormality of the nervous system Aortic aneurysm Hyperpigmentation of the skin Pulmonary arterial hypertension Lymphadenopathy Muscle cramps Brain atrophy Ptosis Peripheral axonal neuropathy Cardiomyopathy Diabetes mellitus Motor delay Hypogonadotrophic hypogonadism Ventriculomegaly Abnormality of the dentition Kyphosis Psychosis Hyporeflexia Type II diabetes mellitus Osteoporosis Hypogonadism Abnormality of the cardiovascular system Adrenal insufficiency Autism Amenorrhea Specific learning disability Hip dysplasia Apnea Abnormality of the pinna Stroke Pruritus Carious teeth Polymicrogyria Cognitive impairment Pulmonary embolism Elevated serum creatine phosphokinase Rhabdomyolysis Abdominal pain Jaundice Hypertrophic cardiomyopathy Dilated cardiomyopathy Leukopenia Hepatic failure Polyneuropathy Decreased liver function Chorioretinal atrophy Multiple lipomas Reduced consciousness/confusion Hypothermia Abnormality of acid-base homeostasis Skeletal muscle atrophy Respiratory distress Arrhythmia Sudden cardiac death Hypercalciuria Inflammation of the large intestine Hyperthyroidism Psychotic episodes Heart block Glomerulopathy Dementia Subcutaneous nodule Hypermetropia Thrombocytopenia Dysphagia Oligomenorrhea Diabetes insipidus Nephritis Involuntary movements Muscle weakness Abnormality of the cerebrospinal fluid Retinal dystrophy Scarring Dry skin Rod-cone dystrophy Renal tubular dysfunction Dysphasia Polydipsia Portal hypertension Growth abnormality Type I diabetes mellitus Malabsorption Nephrotic syndrome Intellectual disability, mild Congenital cataract Gait disturbance Bilateral sensorineural hearing impairment Blurred vision Hyponatremia Growth hormone deficiency Confusion Cranial nerve paralysis Pallor Nausea and vomiting Full cheeks Sepsis Hypopnea Renal Fanconi syndrome Narrow palm Tubulointerstitial abnormality Hypoplastic labia minora Central adrenal insufficiency Abnormality of the cerebellar vermis Gastrointestinal hemorrhage Temperature instability Poor gross motor coordination Triangular mouth Crohn's disease Disseminated intravascular coagulation Erysipelas Frontal upsweep of hair Clitoral hypoplasia Esotropia Anteverted ears Poor fine motor coordination Abdominal obesity Almond-shaped palpebral fissure Oligohydramnios Generalized hypopigmentation Areflexia Morphological abnormality of the inner ear EEG abnormality Gastroesophageal reflux Acidosis Gait ataxia Cerebral cortical atrophy Myoclonus Amaurosis fugax Cerebellar hypoplasia Tapered finger Constipation Delayed skeletal maturation Encephalopathy Acromicria Depressivity Dystonia Hypertonia Diarrhea Sleep disturbance Short neck Auditory hallucinations Respiratory insufficiency Optic atrophy Abnormal nerve conduction velocity Dysarthria Hyperreflexia Hypertelorism Cor pulmonale Chromosome breakage Hemeralopia Increased body weight Nasal speech Poor suck Infantile muscular hypotonia Scrotal hypoplasia Spotty hypopigmentation Sleep apnea Bicuspid aortic valve Paronychia Narrow palpebral fissure Spontaneous abortion Abnormal mitochondrial morphology Edema of the dorsum of hands Cochlear malformation Precocious puberty Aortic valve stenosis Progressive night blindness Bradycardia Insulin resistance Clumsiness Primary amenorrhea Cochlear degeneration Homonymous hemianopia Abnormal mitochondrial shape Narrow forehead Decreased fetal movement Paralytic ileus Failure to thrive in infancy Hyperinsulinemia Ocular albinism Bilateral intracranial calcifications Abnormal cochlea morphology Hypoplasia of the fovea Acrocyanosis Overweight Central hypotonia Abnormality of lipid metabolism Iris hypopigmentation Hypoventilation Hypopigmentation of hair Morphological abnormality of the vestibule of the inner ear Febrile seizures Striae distensae Myeloid leukemia Radial deviation of finger Episodic quadriplegia Narrow nasal bridge Polyphagia External genital hypoplasia Truncal obesity Decreased muscle mass Abnormal macular morphology Skeletal muscle hypertrophy Albinism Glucose intolerance Large hands Emotional lability Impaired pain sensation Generalized tonic-clonic seizures Myalgia Facial diplegia Abnormality of mitochondrial metabolism Posterior subcapsular cataract Hemiplegia Bilateral ptosis Transient ischemic attack Delusions Decreased nerve conduction velocity Cachexia Atrioventricular block Easy fatigability Cardiorespiratory arrest Hyperkinesis Aortic dissection Mitochondrial myopathy Goiter Schizophrenia Mutism Hypopigmented skin patches Ischemic stroke Ragged-red muscle fibers Visual hallucinations Increased CSF lactate Wolff-Parkinson-White syndrome Reduced tendon reflexes Cerebral ischemia Gait imbalance Anterior hypopituitarism Progressive external ophthalmoplegia Ophthalmoparesis Small hand Hyperkalemia Atopic dermatitis Drowsiness Distal arthrogryposis Hashimoto thyroiditis Primary adrenal insufficiency Abnormality of immune system physiology Thyroiditis Basal ganglia calcification Progressive sensorineural hearing impairment Vertebral fusion Prolonged QT interval Visual field defect Vestibular dysfunction Vitiligo Aphasia Bundle branch block Overlapping toe Abnormality of neuronal migration Focal segmental glomerulosclerosis Hemiplegia/hemiparesis Mask-like facies Bifid scrotum Aplasia/Hypoplasia of the cerebellum Abnormality of visual evoked potentials Intestinal obstruction Personality changes Neonatal hypoglycemia Stroke-like episode Seborrheic dermatitis Gastroparesis Leber optic atrophy Memory impairment Increased serum lactate Muscle fiber atrophy Migraine Sensory impairment Writer's cramp Generalized myoclonic seizures Abnormal cerebellum morphology Postural instability Hirsutism Lactic acidosis Persistence of primary teeth Vertigo Dysesthesia Paresthesia Dysmetria Anal atresia Spontaneous hematomas Ophthalmoplegia Arthrogryposis multiplex congenita Lethargy Neurological speech impairment Protruding ear Developmental regression Feeding difficulties in infancy Mental deterioration Anxiety Psychomotor deterioration Cerebral calcification External ophthalmoplegia Hallucinations Left ventricular failure Pancreatitis Speech apraxia Macular degeneration Purpura Exercise intolerance Generalized hirsutism EMG abnormality Retinal pigment epithelial atrophy Truncal ataxia Cardiac arrest Clonus Cerebral visual impairment Gingival overgrowth Motor polyneuropathy Left ventricular hypertrophy Hypertrichosis Hemiparesis Atrial fibrillation Ventricular hypertrophy Abnormality of peripheral nerve conduction Proximal tubulopathy Ileus Hemianopia Status epilepticus Abnormality of the renal tubule Episodic vomiting Generalized-onset seizure Short foot Abnormality of the pleura Downturned corners of mouth Diffuse glomerular basement membrane lamellation Pericarditis Keratitis Skin ulcer Limitation of joint mobility Skin rash Camptodactyly of finger Arthralgia Cylindruria Morphological abnormality of the semicircular canal Lentiglobus Anterior lenticonus Diffuse leiomyomatosis Neoplasm of the colon Abnormality of the optic nerve Uterine neoplasm Lenticonus Thickening of the glomerular basement membrane Macroscopic hematuria Periorbital edema Elliptocytosis Abdominal situs inversus Foam cells Corneal erosion Edema of the lower limbs Microscopic hematuria Macular dystrophy Tinnitus Abnormal cranial nerve morphology Abnormality of the retinal vasculature Hematuria Microdontia Macrocephaly Numerous pigmented freckles Seborrheic keratosis Cholangiocarcinoma Defective DNA repair after ultraviolet radiation damage Morphological abnormality of the central nervous system Verrucae Tubular atrophy Freckling Neoplasm of the skin Bone marrow hypocellularity Cafe-au-lait spot Prominent nose Synovitis Delayed myelination Chorea Progressive cerebellar ataxia Astigmatism Deeply set eye Flexion contracture Abnormal inflammatory response Retrobulbar optic neuritis Large vessel vasculitis Clear cell renal cell carcinoma Polyarticular arthritis Abnormal choroid morphology Posterior uveitis Corneal dystrophy Midface retrusion Elevated hepatic transaminase Normochromic anemia Aciduria Corneal opacity Abnormal pyramidal sign Abnormal static automated perimetry test Abnormal caudate nucleus morphology Thunderclap headache Abnormal kinetic perimetry test Bitemporal hemianopia Trigeminal neuralgia Prolactin deficiency Mydriasis Galactorrhea Central diabetes insipidus Stereotypy Adrenocorticotropic hormone deficiency Pituitary hypothyroidism Excessive daytime somnolence Pituitary adenoma Prolactin excess Increased circulating cortisol level Growth hormone excess Hypopituitarism Impotence Hypergonadotropic hypogonadism Diplopia Hypotension Reduced visual acuity Dehydration Aminoaciduria Exudative retinopathy Premature ovarian insufficiency Multiple small medullary renal cysts Azotemia Abnormality of bone mineral density Tapetoretinal degeneration Congenital hepatic fibrosis Retinal dysplasia Peripheral visual field loss Severe sensorineural hearing impairment Congenital blindness High hypermetropia Nephronophthisis Polyuria Cone-shaped epiphysis Incoordination Hypokalemia Hepatic fibrosis Renal dysplasia Progressive visual loss Renal cyst Retinal degeneration Abnormality of the kidney Abnormality of the skeletal system Elevated intracellular cystine Retinal pigment epithelial mottling Nephrogenic diabetes insipidus Corneal crystals Hypophosphatemia Rickets Abnormality of metabolism/homeostasis Hepatic steatosis Short palm Posterior vitreous detachment Pulmonary granulomatosis Vitreous snowballs Enlarged lacrimal glands Maculopapular exanthema Abnormality of the nasal mucosa Increased T cell count Abnormal cardiac ventricular function Parotitis Abnormal liver parenchyma morphology Non-caseating epithelioid cell granulomatosis Abnormality of T cell physiology Enlargement of parotid gland Abnormality of skin morphology Micrognathia Abnormal reproductive system morphology Vitritis Vitreous floaters Abnormal conjunctiva morphology Anterior uveitis Dacryocystitis Chorioretinitis Abnormality of the adrenal glands Abnormality of the lymph nodes Skin plaque Generalized lymphadenopathy Cystoid macular edema Chylothorax Abnormal trabecular meshwork morphology Strabismus Pneumothorax Prominent forehead Arachnodactyly Infertility Genu valgum Dolichocephaly Leukemia Respiratory tract infection Neonatal hypotonia Thin upper lip vermilion Osteopenia Narrow mouth Micropenis Respiratory failure Upslanted palpebral fissure Recurrent respiratory infections Abnormal facial shape Clinodactyly Obesity Dilatation Syndactyly Short nose Behavioral abnormality Intellectual disability, severe Talipes equinovarus Epicanthus Depressed nasal bridge Delayed speech and language development High palate Cryptorchidism Vitreous hemorrhage Anterior synechiae of the anterior chamber Metabolic acidosis Abnormal chorioretinal morphology Hemolytic anemia Cough Arthritis Proximal muscle weakness Alopecia 3-hydroxydicarboxylic aciduria Decreased activity of 3-hydroxyacyl-CoA dehydrogenase Posterior staphyloma Reye syndrome-like episodes Acute hepatic steatosis Elevated plasma acylcarnitine levels Gastrointestinal inflammation Hepatic encephalopathy Syncope Abnormal left ventricle morphology Decreased plasma carnitine Cholestatic liver disease Hypoketotic hypoglycemia Recurrent hypoglycemia Preeclampsia Loss of consciousness Abnormal electroretinogram Tachypnea Hypocalcemia Sensorimotor neuropathy Exotropia Peripheral demyelination Chest pain Pancytopenia Night sweats Interstitial pulmonary abnormality Skin nodule Bone cyst Immune dysregulation Macular edema Upper airway obstruction Abnormality of the gastrointestinal tract Increased CSF protein Uveitis Optic neuropathy Hemoptysis Keratoconjunctivitis sicca Hyperuricemia Abnormality of the musculature Elevated erythrocyte sedimentation rate Palpitations Increased antibody level in blood Pulmonary fibrosis Emphysema Epiphora Pleural effusion Hypercalcemia Eosinophilia Ventricular tachycardia Osteolysis Nephrocalcinosis Bronchiectasis Nephrolithiasis Abnormal lung morphology Prominent ear helix


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