Hereditary hemorrhagic telangiectasia: diagnosis and management
AM Cuesta - Journal of Clinical Medicine, 2022 - mdpi.com
To date, three subtypes of HHT have been described. HHT type 1 refers to mutations of the
endoglin gene ENG; HHT type 2 refers to mutations of the activin A receptor, similar to the …
endoglin gene ENG; HHT type 2 refers to mutations of the activin A receptor, similar to the …
HHT-Related Epistaxis and Pregnancy—A Retrospective Survey and Recommendations for Management from an Otorhinolaryngology Perspective
KEC Andorfer, CT Seebauer, C Dienemann… - Journal of Clinical …, 2022 - mdpi.com
Appropriate management of hereditary hemorrhagic telangiectasia (HHT) is of particular
importance in females, as HHT-mediated modifications of the vascular bed and circulation …
importance in females, as HHT-mediated modifications of the vascular bed and circulation …
Hereditary Hemorrhagic Telangiectasia Associating Neuropsychiatric Manifestations with a Significant Impact on Disease Management—Case Report and Literature …
(1) Background: Genetic hereditary hemorrhagic telangiectasia (HHT) is clinically
diagnosed. The clinical manifestations and lack of curative therapeutic interventions may …
diagnosed. The clinical manifestations and lack of curative therapeutic interventions may …
[HTML][HTML] Hereditary Hemorrhagic Telangiectasia With Multiple Ear, Nose, and Throat (ENT) Manifestations: A Case Report
E Litsou, L Basiari, G Tsirves, GV Psychogios - Cureus, 2023 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber
syndrome, is a rare autosomal dominant multisystem disorder. It is a mucocutaneous and …
syndrome, is a rare autosomal dominant multisystem disorder. It is a mucocutaneous and …
Hemoraginė paveldima telangiektazija otorinolaringologijoje: etiopatogenezė, diagnostika ir gydymas
T Kavaliauskaitė - 2023 - epublications.vu.lt
Abstract [eng] Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder
associated with alterations of angiogenesis. Heterozygous mutations in the ENG or ACVRL1 …
associated with alterations of angiogenesis. Heterozygous mutations in the ENG or ACVRL1 …
[PDF][PDF] Experience with Argon Plasma Coagulation in Treatment of Recurrent Epistaxis in Patients with Hereditary Hemorrhagic Telangiectasia
F Alžběta, L Dostálová, J Plzák - B-ENT, 2022 - b-ent.be
Objective: Hereditary hemorrhagic telangiectasia, or Rendu-Osler-Weber disease, is an
autosomal dominant genetic disorder characterized by abnormal vessel formation …
autosomal dominant genetic disorder characterized by abnormal vessel formation …