| Autor: |
Kaur, Bhavneet, Boorugu, Hari K., Ravishankar, Usha, Devi, Sailaja |
| Předmět: |
|
| Zdroj: |
Journal of Postgraduate Medicine, Education & Research; Jan-Mar2024, Vol. 58 Issue 1, p24-26, 3p |
| Abstrakt: |
Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder characterized by angiodysplasia which may manifest with telangiectasia and arteriovenous malformations (AVMs) in the central nervous system, lung, liver, and gastrointestinal tract. Women suffering from HHT may have a normal pregnancy course but some pregnancies are at risk of fulminant complications related to hormonal and cardiovascular changes of pregnancy. Hence, it becomes very important to diagnose this condition promptly and monitor women with HHT carefully to reduce morbidity and mortality associated with the disease. We present two women diagnosed with HHT in pregnancy who presented to our institution with different clinical scenarios. Based on the clinical findings, family history and high index of suspicion, we were able to diagnose and manage them accordingly. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
