telangiectasia in English

noun
1
a condition characterized by dilation of the capillaries, which causes them to appear as small red or purple clusters, often spidery in appearance, on the skin or the surface of an organ.
Tortuous dilation of the hepatic arteries and capillary telangiectasia of the hepatic surface in the operative field were remarkable.

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1. Ataxia-telangiectasia (AT) is a rarer type of hereditary Ataxia

2. Diseases associated with Atm include Ataxia-Telangiectasia and Mantle Cell Lymphoma

3. Ataxia-telangiectasia is a rare genetic condition that affects the nervous system, immune system and other body systems

4. Ataxia-telangiectasia (A-T) is an autosomal recessive, complex, multisystem disorder characterized by progressive neurologic impairment, cerebellar Ataxia, variable immunodeficiency with susceptibility to sinopulmonary infections, impaired organ maturation, x-ray hypersensitivity, ocular and cutaneous telangiectasia (see image below), and a predisposition to malignancy.

5. Ataxia telangiectasia (AT) is the most common form of infantile-onset cerebellar Ataxia, with a prevalence estimated at 1-2.5 per 100,000

6. The worst side effects are hypopigmentation, telangiectasia and Cicatrization (see Figure 1), and hyperpigmentation and in particular loss of elasticity in the skin field treated

7. Acute or chronic upper gastrointestinal (UGI) bleeding and iron deficiency anemia may result from UGI Angiomata. In this report, specific angiomatous lesions discussed are Osler-Weber-Rendu (O-W-R) telangiectasia and other Angiomata.

8. Capillary Telangiectasia (CTS) is a type of vascular malformation of the brain, in which clusters of dilated capillaries are formed in some areas of the brain, interspersed with normal brain tissue.

9. This page includes the following topics and synonyms: Cell-Mediated Immunodeficiency, Cell mediated Immunity Disorder, T-Cell Disorder, Severe Combined Immunodeficiency, SCID, Ataxia Telangiectasia, Wiscott-Aldrich Syndrome, DiGeorge Syndrome, Velocardiofacial Syndrome, Congenital Thymic Aplasia.

10. Atavistic; Atavistic epiphysis; Atavistic regression; ataxaphasia; ataxia; ataxia neuropathy spectrum; ataxia of Charlevoix-Saguenay; ataxia of early onset with retained reflexes; ataxia paramyotonia; ataxia telangiectasia; ataxia telangiectasialike disorder; ataxia with infantile onset olivopontocerebellar atrophy; ataxia with isolated vitamin

11. Crest (calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome is a member of the heterogeneous group of sclerodermas, and its name is an acronym for the cardinal clinical features of the syndrome.[1, 2] In 1910, Thibierge and Weissenbach described the first case report of what was later called CRST (calcinosis cutis, Raynaud phenomenon