Hereditary benign telangiectasia?

نویسنده

  • Şinasi Özsoylu
چکیده

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Hereditary benign Telangiectasia: Report of 6 cases in a family

Hereditary benign telangiectasia is an uncommon idiopathic skin disorder characterized by generalized telangiectases and angiomatous lesions of the skin. The diagnosis should be suspected in patients with such cutaneous lesions, positive family history, no associated bleeding problems, and no mucosal involvement. We present six cases of hereditary benign telangiectasia in three generations of o...

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Peliosis hepatis associated with hereditary haemorrhagic telangiectasia

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal, predominantly inherited disease characterized by diffuse telangiectases involving the skin, mucous membranes, lung, brain, gastrointestinal tract and liver. Peliosis hepatis is a rare, benign disorder causing sinusoidal dilatation and the presence of multiple blood-filled lacunar spaces within the liver. We report a case of an HHT pa...

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Hereditary benign telangiectasia--first family in Northern Ireland.

Hereditary benign telangiectasia (HBT), first described in 1971,1 is a rare autosomal dominant disorder.2' 3, 4 It is characterised by widespread telangiectases which may be punctate, plaquelike, radiating or merely a diffuse blush. The lesions generally are observed before adolescence, and rarely during the first year of life.5 It is important to recognise HBT as it may only cause cosmetic dis...

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LETTER TO JMG Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14

T elangiectases are characterised by an abnormal permanent dilatation of end vessels—mainly venules but occasionally also capillaries and arterioles—in the subpapillary plexus in the upper part of the dermis. Hereditary benign telangiectasia (HBT; OMIM 187260) is a rare genetic skin disorder classified among the primary or idiopathic telangiectases. Affected individuals present with widespread ...

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Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14.

T elangiectases are characterised by an abnormal permanent dilatation of end vessels—mainly venules but occasionally also capillaries and arterioles—in the subpapillary plexus in the upper part of the dermis. Hereditary benign telangiectasia (HBT; OMIM 187260) is a rare genetic skin disorder classified among the primary or idiopathic telangiectases. Affected individuals present with widespread ...

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عنوان ژورنال:
  • The Turkish journal of pediatrics

دوره 57 6  شماره 

صفحات  -

تاریخ انتشار 2015