Results 101 to 110 of about 4,853 (149)

Assessing racial differences in North American hereditary hemorrhagic telangiectasia study recruitment and care. [PDF]

Orphanet J Rare Dis
Scott G, Agundiz A, Nelson J, Hetts S, Clancy M, Kim H, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group.   +7 more
europepmc   +1 more source

Family planning, sexual activity and contraception in hereditary hemorrhagic telangiectasia: a European survey study. [PDF]

Orphanet J Rare Dis
Hessels J, Post MC, Boerman S, Droege F, Dupuis O, ePAG, Geisthoff UW, Haahr PD, Kjeldsen AD, Mager JJ, Dupuis-Girod S, Buscarini E.   +11 more
europepmc   +1 more source

When Cholangitis Reveals Liver Involvement in Hereditary Hemorrhagic Telangiectasia: A Case Report. [PDF]

Cureus
El Graini S, Oukassem S, Retal H, Nassar I, Imrani K.   +4 more
europepmc   +1 more source

Coexistence of Hereditary Hemorrhagic Telangiectasia and Moyamoya Disease: A Case Report Highlighting a Potential Genetic Synergy. [PDF]

Appl Clin Genet
Liu S, Meng L, Wan Y, Liu S, Shi L.
europepmc   +1 more source

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Hereditary Hemorrhagic Telangiectasia

Otolaryngologic Clinics of North America, 2018
Hereditary hemorrhagic telangiectasia (HHT) describes the presenting manifestations of a disorder that is characterized by pathologic blood vessels. HHT is inherited as an autosomal dominant trait with variable penetrance. The abnormal vascular structures (dysplasias) can affect all the organs in the human body. The link between a physical stimulus and
Thomas, Kühnel, Kornelia, Wirsching, Walter, Wohlgemuth, Ajay, Chavan, Katja, Evert, Veronika, Vielsmeier   +5 more
  +6 more sources

Hereditary hemorrhagic telangiectasia

Oral Surgery, Oral Medicine, Oral Pathology, 1965
Abstract Two cases of hereditary hemorrhagic telangiectasia in Negro patients have been reported. Both cases could be considered classic with respect to the oral lesions and familial history. Although numerous oral lesions and chronic epistaxis were present, severe, persistent anemia was the primary problem to be dealt with in both cases.
R M, SMITH, M, ROBBINS
openaire   +2 more sources

Hereditary Hemorrhagic Telangiectasia

Ophthalmic Plastic & Reconstructive Surgery, 1990
A patient with hereditary hemorrhagic telangiectasia and bloody tears is described. This case report serves to familiarize the ophthalmic plastic and reconstructive surgeon with the differential diagnosis of bloody tears. Conjunctival, oral mucosal and cutaneous findings are documented, and the systemic and ocular manifestations of hereditary ...
S H, Goldberg, J D, Bullock
openaire   +2 more sources

Hereditary Hemorrhagic Telangiectasia

Clinics in Chest Medicine, 2016
Hereditary hemorrhagic telangiectasia (HHT) is an underrecognized and underdiagnosed autosomal-dominant angiodysplasia that has an estimated prevalence of 1 in 5000 individuals, with variable clinical presentations even within family members with identical mutations.
openaire   +3 more sources

Hereditary Hemorrhagic Telangiectasia

New England Journal of Medicine, 1995
Identified nearly a century ago, hereditary hemorrhagic telangiectasia, or Rendu–Osler–Weber syndrome, has long been viewed as a rare condition producing minor discomfort for affected persons. However, this disorder is now considered to be more common than previously thought,1–5 and the associated brain and pulmonary lesions are sources of substantial ...
A E, Guttmacher, D A, Marchuk, R I, White   +2 more
openaire   +2 more sources

Hereditary hemorrhagic telangiectasia/avastin

The Laryngoscope, 2009
Abstract This is the first scientific report of hereditary hemorrhagic telangiectasia (HHT) epistaxis treatment by intranasal spraying of the vascular endothelial growth factor (VEGF) inhibitor bevacizumab (Avastin). Epistaxis in patients with HHT is a morbid, mortal condition that is difficult and unpleasant to manage.
Terence M, Davidson, Scott E, Olitsky, Julie L, Wei   +2 more
openaire   +2 more sources