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Small dilated blood vessels
Telangiectasias (from tel- 'end', angi- 'blood vessel' and ectasia 'the expansion of a hollow or tubular organ'), also known as spider veins, are small
Telangiectasia
Connective tissue disorder
calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia. CREST syndrome is associated with detectable antibodies against centromeres
CREST_syndrome
Genetic disorder affecting blood vessel development
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu disease and Osler–Weber–Rendu syndrome, is a rare autosomal dominant genetic
Hereditary hemorrhagic telangiectasia
Hereditary_hemorrhagic_telangiectasia
Rare neurodegenerative disease
Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis-Bar syndrome, is a rare, neurodegenerative disease causing
Ataxia–telangiectasia
Disease of the retina affecting central vision
juxtafoveal telangiectasia: macular telangiectasia type 1, macular telangiectasia type 2, and macular telangiectasia type 3. Both macular telangiectasia and age-related
Macular_telangiectasia
Medical condition
Generalized essential telangiectasia, also known as general essential telangiectasia, is characterized by the dilation of veins and capillaries over a
Generalized essential telangiectasia
Generalized_essential_telangiectasia
Medical condition
Unilateral nevoid telangiectasia presents with fine thread veins, typically over a segment of skin supplied by a particular nerve on one side of the body
Unilateral nevoid telangiectasia
Unilateral_nevoid_telangiectasia
Medical condition
Hypotrichosis–lymphedema–telangiectasia syndrome is a congenital syndrome characterized by lymphedema (swelling of tissue due to malformation or malfunction
Hypotrichosis–lymphedema–telangiectasia syndrome
Hypotrichosis–lymphedema–telangiectasia_syndrome
Human disease
Telangiectasia macularis eruptiva perstans (TMEP) is persistent, pigmented, asymptomatic eruption of macules usually less than 0.5 cm in diameter with
Telangiectasia macularis eruptiva perstans
Telangiectasia_macularis_eruptiva_perstans
Mammalian protein found in Homo sapiens
ATM serine/threonine kinase or Ataxia-telangiectasia mutated, symbol ATM, is a serine/threonine protein kinase that is recruited and activated by DNA double-strand
ATM_serine/threonine_kinase
Small bright red dome-shaped bump on the skin
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Cherry_angioma
Ballooning or rupturing of a blood vessel in the brain
neoplasia type I, pseudoxanthoma elasticum, hereditary hemorrhagic telangiectasia and Ehlers-Danlos syndrome types II and IV. Specific genes have also
Intracranial_aneurysm
Medical condition in which superficial veins become large and twisted
leader Gaius Marius. Aching, heavy legs Appearance of spider veins (telangiectasia) in the affected leg Ankle swelling A brownish-yellow shiny skin discoloration
Varicose_veins
Inflammation of the veins
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Phlebitis
Medical condition
angioma Other names Nevus araneus, spider nevus, vascular spider, spider telangiectasia Non-benign angiomas indicating cirrhosis Specialty Dermatology
Spider_angioma
Oxygen shortage of the brain
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Cerebral_hypoxia
Medical condition
NBS1 gene. Unsurprisingly, many of the features are similar to ataxia telangiectasia (AT) and this syndrome was sometimes termed AT-variant 1, as the protein
Nijmegen_breakage_syndrome
Gene therapy medication
encapsulated cell-based gene therapy used for the treatment of macular telangiectasia type 2. Revakinagene taroretcel is administered into the recipient's
Revakinagene_taroretcel
Drop in blood pressure when standing up or sitting down
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Orthostatic_hypotension
Abnormal connection between arteries and veins, bypassing the capillaries
infection. They are most commonly associated with hereditary hemorrhagic telangiectasia. AVMs are usually congenital and are part of the RASopathy family of
Arteriovenous_malformation
Ataxia-telangiectasia group D complementing (ATDC) is a gene implicated in ataxia-telangiectasia. It is involved in a mouse model of pancreatic cancer
Ataxia-telangiectasia group D complementing
Ataxia-telangiectasia_group_D_complementing
Rare neurodegenerative disease
encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary
ALS
Inflammatory disease involving a buildup of lesions in the walls of arteries
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Atherosclerosis
Long-term high blood pressure in the arteries
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Hypertension
Thickening, hardening and loss of elasticity of the walls of arteries
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Arteriosclerosis
Abnormal enlargement of the pampiniform plexus veins in the scrotum
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Varicocele
Any medical condition that affects the integumentary system
applied to the body with elongated objects without sharp edges. Telangiectasia: A telangiectasia represents an enlargement of superficial blood vessels to the
Skin_condition
Medical condition in which spasm of arteries causes episodes of reduced blood flow
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Raynaud_syndrome
Inability to coordinate movement of the esophagus
calcinosis, Raynaud syndrome, esophageal dysmotility, sclerodactyly and telangiectasia. The most common symptom of esophageal motility disorders is dysphagia
Esophageal_motility_disorder
Abnormally low blood pressure
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Hypotension
Inflammation of the eyelid
eyelashes and/or growth misdirection, trichiasis. Other signs may include telangiectasia on the anterior eyelid, collarettes encircling the lash base, and corneal
Blepharitis
Excessive enlargement of the human aorta
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Aortic_aneurysm
Blood vessels that carry blood towards the heart
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Vein
Localized enlargement of the abdominal aorta
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Abdominal_aortic_aneurysm
Medication
side effects include skin irritation, dry skin, redness, pimples, and telangiectasia. More serious side effects include allergic reactions, cellulitis, adrenal
Clobetasol_propionate
Inflammation or infection of the lymphatic channels
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Lymphangitis
Formation of blood clots inside the blood vessels
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Thrombosis
Blockage of an artery in the lungs
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Pulmonary_embolism
Skin condition, usually on the face
ears (otophyma). Telangiectasias may be present. In ocular rosacea, affected eyes and eyelids may appear red due to telangiectasias and inflammation,
Rosacea
Protein kinase that detects DNA damage and halts cell division
Serine/threonine-protein kinase ATR, also known as ataxia telangiectasia and Rad3-related protein (ATR) or FRAP-related protein 1 (FRP1), is an enzyme
Ataxia telangiectasia and Rad3 related
Ataxia_telangiectasia_and_Rad3_related
Class of enzymes
involving the nervous system. Mutations in the ATM gene cause ataxia–telangiectasia. The ATM gene provides instructions for making a protein that helps
DNA_ligase
sequences on exon 7. Mutations in the ATM gene are responsible for ataxia telangiectasia. These mutations are generally single base pair substitutions, deletions
Exonic_splicing_silencer
Steroid medication
some of the ataxia (poor coordination) symptoms associated with ataxia telangiectasia (A-T) by 28-31%. Betamethasone is also used to stimulate fetal maturation
Betamethasone
American rock band
the caption "W.C. Fields with gin blossoms", referring to the actor's telangiectasia-spotted face and rhinophymic nose by the slang term for the skin condition
Gin_Blossoms
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
May–Thurner_syndrome
Orphan disease
patients share five characteristics from which the acronym is derived: telangiectasias, elevated erythropoietin and erythrocytosis, monoclonal gammopathy
TEMPI_syndrome
Medical condition
encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary
Restless_legs_syndrome
Excessive production of lymphocytes by the immune system
X-linked recessive disorder), and ataxia–telangiectasia.[citation needed] Even though ataxia telangiectasia is an autosomal recessive disorder, people
Lymphoproliferative_disorders
Any impairment or discomfort in walking
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Claudication
Medical sign
distribution, which may progress and become poikilodermatous (atrophic with telangiectasia and pigmentary changes) and indurated (as a result of mucin deposition)
Gottron's_sign
Skin thinning due to prolonged exposure to topical steroids
further and deeper topical steroid side effects may occur, such as telangiectasia, easy bruising, purpura, and striae. Intralesional steroids may result
Steroid-induced_skin_atrophy
Blockage of a blood vessel by a circulatory mass (embolus)
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Embolism
Injury to the innermost layer of the aorta
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Aortic_dissection
Pressure exerted by circulating blood upon the walls of arteries
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Blood_pressure
Disease involving heart or blood vessels
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Cardiovascular_disease
Reduction of blood flow to the heart
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Coronary_artery_disease
Vascular structures in the anal canal
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Hemorrhoid
Medical condition
syndromes (CBSs), and B-cell and T-cell combined disorders such as ataxia-telangiectasia (AT) and Wiskott–Aldrich syndrome (WAS). Recognition of T cell disorders
T_cell_deficiency
Effect of alcohol consumption on the human body
capillaries are excessively reactive, leading to redness from flushing or telangiectasia. Rosacea has been mistakenly attributed to alcoholism because of its
Alcohol_flush_reaction
Ocular route of drug administration
triamcinolone acetonide (a corticosteroid) in the treatment of macular telangiectasia type 1. Also, it is used in the ocular anesthesia. Calenda, Emile; Olle
Sub-Tenon_injection
Bulge in the wall of a blood vessel
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Aneurysm
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
List of ICD-9 codes 390–459: diseases of the circulatory system
List_of_ICD-9_codes_390–459:_diseases_of_the_circulatory_system
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Stenosis
Neurological impairment of voluntary muscle movement
absorbed dose of more than 30 grays. Furthermore, those with ataxia telangiectasia may have a high sensitivity towards gamma rays and x-rays. Vitamin B12
Ataxia
Tissue damage after return of blood supply following ischemia or hypoxia
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Reperfusion_injury
Obstruction of a blood vessel by a clot
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Thromboembolism
Pharmaceutical compound
cancer. It is a selective oral small molecule inhibitor of ATR (Ataxia telangiectasia and Rad3 related), developed by Repare Therapeutics. This drug targets
Camonsertib
Skin rash resulting from excess exposure to heat
development of reticulated erythema, hyperpigmentation, scaling, and telangiectasias in the affected area. Some people may complain of mild itchiness and
Erythema_ab_igne
Increased blood pressure in lung arteries
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Pulmonary_hypertension
Addition of hydrogen atoms to fat molecules
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Fat_hydrogenation
When a kinase phosphorylates itself
Autophosphorylation is a type of post-translational modification of proteins. It is generally defined as the phosphorylation of the kinase by itself. In
Autophosphorylation
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Pulmonary venoocclusive disease
Pulmonary_venoocclusive_disease
Dilated veins in the lower oesophagus
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Esophageal_varices
Medication
common side effects include headache, epistaxis (nosebleed), rash, telangiectasia (spider veins), diarrhea, dizziness, and erythema (redness of the skin)
Sotatercept
hole, and age-related macular degeneration. Macular dystrophies and telangiectasia are among the less common causes. "Can macular scarring due to an infection
Macular_scarring
Absence or defect of controlled, voluntary, and purposeful eye movement
a deficiency in the immune system. Ataxia telangiectasia results from defects in the ataxia telangiectasia mutated gene, which can cause abnormal cell
Oculomotor_apraxia
Protein-coding gene in humans
Mutations in this gene are associated with hereditary hemorrhagic telangiectasia (HHT) type 2, also known as Rendu-Osler-Weber syndrome 2. Germline mutations
ACVRL1
Loss of elasticity in blood vessels
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Arterial_stiffness
American actor and filmmaker (born 1972)
ten-year-old Joe Kindregan (1988–2015), who had the rare disease ataxia-telangiectasia (A-T), and his family. He became actively involved in fundraising for
Ben_Affleck
Progressive neurological disease
disorders in which ataxia is a prominent feature: Friedreich ataxia, ataxia-telangiectasia, ataxia with vitamin E deficiency, ataxia with oculomotor apraxia (AOA)
Spinocerebellar_ataxia
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Degos_disease
Topics referred to by the same term
psychological method Antithrombin, a small protein molecule Ataxia–telangiectasia, an immunodeficiency disorder Athletic training Atrial tachycardia Astatine
AT
Medical intervention
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Flow_diverter
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Pituitary_apoplexy
Accumulation of degenerative material in the inner layer of artery walls
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Atheroma
Visual impairment caused by a brain problem
encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary
Cortical_visual_impairment
Medical condition
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Acute_aortic_syndrome
Group of inherited conditions
following chromosome instability syndromes are known: Ataxia telangiectasia Ataxia telangiectasia-like disorder Bloom syndrome Fanconi anaemia Nijmegen breakage
Chromosome instability syndrome
Chromosome_instability_syndrome
Pooling of blood in the veins
conditions that appears as atrophic plaques of ivory white skin with telangiectasias. It represents late sequelae of lipodermatosclerosis where the skin
Chronic_venous_insufficiency
Type of progressive dementia
encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary
Dementia_with_Lewy_bodies
Benign tumors derived from cells composing or surrounding blood or lymph vessels
(simple) Cavernous (cystic) Glomus tumor Vascular ectasias Naevus flammeus Telangiectasia – spider, hereditary hemorrhagic Reactive vascular proliferations Bacillary
Angioma
Abnormal narrowing of arteries other than those that supply the heart or brain
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Peripheral_artery_disease
Pharmaceutical compound
an experimental anticancer drug which acts as an inhibitor of ataxia telangiectasia and Rad3 related protein. This is involved in DNA repair following damage
Elimusertib
British novelist (1906–1998)
it was discovered she was suffering from a rare vascular disease, telangiectasia, which caused bleeding from the nose, fingers, and stomach and resulted
Catherine_Cookson
Blood cancer characterized by overproduction of lymphoblasts
Shwachman–Diamond syndrome, Kostmann syndrome, neurofibromatosis type 1, ataxia-telangiectasia, paroxysmal nocturnal hemoglobinuria, and Li–Fraumeni syndrome. Fewer
Acute_lymphoblastic_leukemia
Physiological processes of hypertension
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Pathophysiology of hypertension
Pathophysiology_of_hypertension
Visible lesion indicating atherosclerosis
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Fatty_streak
Medical condition
encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary
Cortical_blindness
Formation of blood clots in the deep veins of the arms
fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Generalized essential telangiectasia Vascular nevus Cherry hemangioma
Paget–Schroetter_disease
Hardening of finger or toe skin into a claw-like shape
calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia.) Sclerodactyly is also one component of Huriez Syndrome, along with
Sclerodactyly
TELANGIECTASIA
TELANGIECTASIA
TELANGIECTASIA
TELANGIECTASIA
Girl/Female
Indian, Telugu
Good Light
Boy/Male
Indian
Hawk like
Boy/Male
Hindu, Indian, Marathi
Fast; Progressing; Lord Vishnu
Girl/Female
Arabic, Muslim
Royal Glow
Girl/Female
Hindu, Indian, Telugu
One of the Star; Name of a Gopi of Gukul
Girl/Female
Indian, Tamil
Lustrous
Boy/Male
British, English
Wise
Boy/Male
Hindu, Indian
Gift of God
Female
English
English name derived from the Latin word felinus, FELINA means "cat-like."
Surname or Lastname
English and North German
English and North German : variant of Bertram.William Bartram, a Quaker, had a large farm near Darby, PA, when his eldest son, John, the first American botanist, was born in 1699. John conducted botanical experiments at his own farm in Kingsessing, PA, near Philadelphia.
TELANGIECTASIA
TELANGIECTASIA
TELANGIECTASIA
TELANGIECTASIA
TELANGIECTASIA