U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Search results

Items: 4

1.

Telangiectasia, hereditary hemorrhagic, type 1

Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct connections between arteries and veins. The most common clinical manifestation is spontaneous and recurrent nosebleeds (epistaxis) beginning on average at age 12 years. Telangiectases (small AVMs) are characteristically found on the lips, tongue, buccal and gastrointestinal (GI) mucosa, face, and fingers. The appearance of telangiectases is generally later than epistaxis but may be during childhood. Large AVMs occur most often in the lungs, liver, or brain; complications from bleeding or shunting may be sudden and catastrophic. A minority of individuals with HHT have GI bleeding, which is rarely seen before age 50 years. [from GeneReviews]

MedGen UID:
1643786
Concept ID:
C4551861
Disease or Syndrome
2.

Hereditary hemorrhagic telangiectasia type 4

Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct connections between arteries and veins. The most common clinical manifestation is spontaneous and recurrent nosebleeds (epistaxis) beginning on average at age 12 years. Telangiectases (small AVMs) are characteristically found on the lips, tongue, buccal and gastrointestinal (GI) mucosa, face, and fingers. The appearance of telangiectases is generally later than epistaxis but may be during childhood. Large AVMs occur most often in the lungs, liver, or brain; complications from bleeding or shunting may be sudden and catastrophic. A minority of individuals with HHT have GI bleeding, which is rarely seen before age 50 years. [from GeneReviews]

MedGen UID:
341824
Concept ID:
C1857688
Disease or Syndrome
3.

Fibromuscular dysplasia, multifocal

Multifocal fibromuscular dysplasia (FMDMF) is characterized histologically by medial fibroplasia and angiographically by multiple arterial stenoses with intervening mural dilations. Arterial tortuosity, macroaneurysms, dissections, and rupture may occur (summary by Richer et al., 2020). [from OMIM]

MedGen UID:
1778238
Concept ID:
C5543412
Disease or Syndrome
4.

Dilatation of celiac artery

Abnormal outpouching or sac-like dilatation in the wall of the celiac artery. [from HPO]

MedGen UID:
1393390
Concept ID:
C4477059
Anatomical Abnormality
Format

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity