[HTML][HTML] Multifocal Abscesses, Necrotizing Fasciitis, Iron Deficiency Anemia, and Hypophosphatemia Induced by Ferric Carboxymaltose Infusions: Report of a Case of …
LA Trevise, MPLV Pinto, G Hasselmann… - Cureus, 2023 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant vascular
dysplasia in which disrupted angiogenesis leads to increased formation of mucocutaneous …
dysplasia in which disrupted angiogenesis leads to increased formation of mucocutaneous …
[引用][C] Concurrent Hereditary Hemorrhagic Telangiectasia and Hereditary Hemochromatosis: A Case Report
Background Coexisting hereditary hemorrhagic telangiectasia and hemochromatosis is an
exceedingly rare combination of 2 inherited disorders that provides an advantageous …
exceedingly rare combination of 2 inherited disorders that provides an advantageous …
Iron deficiency anemia related to hereditary hemorrhagic telangiectasia: response to treatment with bevacizumab
JM Fleagle, RK Bobba, CG Kardinal… - The American journal of the …, 2012 - Elsevier
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant condition
associated with arteriovenous malformations (AVMs) or telangiectasias of the pulmonary …
associated with arteriovenous malformations (AVMs) or telangiectasias of the pulmonary …
Iron deficiency anemia related to hereditary hemorrhagic telangiectasia: response to treatment with bevacizumab.
JM Fleagle, RK Bobba, RF Khozouz, P Garg… - Journal of Clinical …, 2011 - ascopubs.org
e13521 Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal
dominant condition associated with arteriovenous malformations or telangiectasia's of the …
dominant condition associated with arteriovenous malformations or telangiectasia's of the …
[HTML][HTML] Hereditary hemorrhagic telangiectasia: a rare cause of anemia
W Jan, ATU Din, FMD Chaudhary, F Nawaz - Cureus, 2019 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasias (HHT), also known as Osler-Weber-Rendu
syndrome, is an uncommon genetic disorder. It is inherited as an autosomal dominant …
syndrome, is an uncommon genetic disorder. It is inherited as an autosomal dominant …
Woman presenting with chronic iron deficiency anemia associated with hereditary hemorrhagic telangiectasia: a case report
P Stross - Drug, Healthcare and Patient Safety, 2013 - Taylor & Francis
Background Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder
associated with frequent nose bleeds that can be troublesome and difficult to contain. A …
associated with frequent nose bleeds that can be troublesome and difficult to contain. A …
Hereditary hemorrhagic telangiectasia
JG Parambil - Clinics in chest medicine, 2016 - chestmed.theclinics.com
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal-dominant disorder that leads
to the formation of dysplastic blood vessels in mucocutaneous surfaces. 1, 2 Dysplastic …
to the formation of dysplastic blood vessels in mucocutaneous surfaces. 1, 2 Dysplastic …
[HTML][HTML] Frontiers in Medical Case Reports (FMCR)
GA Demirjian, LC Tou, SE Sugerik, TA Siddiqui… - jmedicalcasereports.org
Hereditary hemorrhagic telangiectasia (HHT) is a condition known for frequent and severe
epistaxis, telangiectasias that form along various surfaces of the body, and potentially life …
epistaxis, telangiectasias that form along various surfaces of the body, and potentially life …
[HTML][HTML] Hereditary hemorrhagic telangiectasia
A Grand'Maison - CMAJ, 2009 - Can Med Assoc
@@ See related case by Manawadu and colleagues, page 836, and clinical images by
Nanda and Bhatt, page 838, and by Irani and Kasmani, page 839 orrhagic telangiectasia …
Nanda and Bhatt, page 838, and by Irani and Kasmani, page 839 orrhagic telangiectasia …
[HTML][HTML] A rare case of hereditary hemorrhagic telangiectasia: a case report
AR Khan, S Waqar, MH Wazir, A Arif - Cureus, 2022 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu
syndrome, is a very rare autosomal dominant genetic disorder that leads to abnormal blood …
syndrome, is a very rare autosomal dominant genetic disorder that leads to abnormal blood …