Pulmonary Arteriovenous Malformations Unmasked by Refractory Hypoxia: An Unusual Presentation in Hereditary Hemorrhagic Telangiectasia
Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder usually known to manifest with epistaxis, mucocutaneous telangiectasia, and visceral arteriovenous malformations (AVMs). Clinical Description: A 12-year-old girl presented with altered sensorium on hand ventilation, r...
Saved in:
| Main Authors: | Sharmila Sankar, P. S. Rajakumar, S. Shuba, Vimalnath Shanmugam, Sabarish Sekar, Jebaraj Rathinasamy |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2024-11-01
|
| Series: | Indian Pediatrics Case Reports |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/ipcares.ipcares_118_24 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Prospective pilot study of Floseal® for the treatment of anterior epistaxis in patients with hereditary hemorrhagic telangiectasia (HHT)
by: John M. Lee, et al.
Published: (2019-10-01) -
Topical propranolol improves epistaxis in patients with hereditary hemorrhagic telangiectasia - a preliminary report
by: Meir Mei-Zahav, et al.
Published: (2017-10-01) -
The effect of the COVID-19 pandemic on epistaxis and anaemia in patients with hereditary haemorrhagic telangiectasia (HHT) in central South Africa
by: Stephanie Juané Kennedy, et al.
Published: (2025-07-01) -
Leaf anatomy of Celtis iguanaea (Cannabaceae): a contribution to the classification and taxonomy of the species
by: Henrique Borges Zamengo, et al.
Published: (2025-05-01) -
Novel brain arteriovenous malformation mouse models for type 1 hereditary hemorrhagic telangiectasia.
by: Eun-Jung Choi, et al.
Published: (2014-01-01)