Hutchinson - Gilford progeria syndrome: A rare case report
Hutchinson - Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic "plucked-bird" appear...
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Wolters Kluwer Medknow Publications
2014-01-01
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doaj-fb8cd3898ea04047865ff3e76589b4c72020-11-24T21:22:53ZengWolters Kluwer Medknow PublicationsIndian Dermatology Online Journal2229-51782014-01-015447848110.4103/2229-5178.142507Hutchinson - Gilford progeria syndrome: A rare case reportSubhash KashyapVinay ShankerNeeraj SharmaHutchinson - Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic "plucked-bird" appearance, prominent eyes and scalp veins, senile look, loss of scalp hair, eyebrows, and eyelashes, stunted growth, and mottled pigmentation with sclerodermatous changes over the trunk and lower limbs. Radiological changes and decreased high-density lipoprotein (HDL) levels were also characteristic of the syndrome. This interesting case is reported for its rarity.http://www.idoj.in/article.asp?issn=2229-5178;year=2014;volume=5;issue=4;spage=478;epage=481;aulast=KashyapHutchinson - Gilford syndromepremature agingprogeria |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Subhash Kashyap Vinay Shanker Neeraj Sharma |
spellingShingle |
Subhash Kashyap Vinay Shanker Neeraj Sharma Hutchinson - Gilford progeria syndrome: A rare case report Indian Dermatology Online Journal Hutchinson - Gilford syndrome premature aging progeria |
author_facet |
Subhash Kashyap Vinay Shanker Neeraj Sharma |
author_sort |
Subhash Kashyap |
title |
Hutchinson - Gilford progeria syndrome: A rare case report |
title_short |
Hutchinson - Gilford progeria syndrome: A rare case report |
title_full |
Hutchinson - Gilford progeria syndrome: A rare case report |
title_fullStr |
Hutchinson - Gilford progeria syndrome: A rare case report |
title_full_unstemmed |
Hutchinson - Gilford progeria syndrome: A rare case report |
title_sort |
hutchinson - gilford progeria syndrome: a rare case report |
publisher |
Wolters Kluwer Medknow Publications |
series |
Indian Dermatology Online Journal |
issn |
2229-5178 |
publishDate |
2014-01-01 |
description |
Hutchinson - Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic "plucked-bird" appearance, prominent eyes and scalp veins, senile look, loss of scalp hair, eyebrows, and eyelashes, stunted growth, and mottled pigmentation with sclerodermatous changes over the trunk and lower limbs. Radiological changes and decreased high-density lipoprotein (HDL) levels were also characteristic of the syndrome. This interesting case is reported for its rarity. |
topic |
Hutchinson - Gilford syndrome premature aging progeria |
url |
http://www.idoj.in/article.asp?issn=2229-5178;year=2014;volume=5;issue=4;spage=478;epage=481;aulast=Kashyap |
work_keys_str_mv |
AT subhashkashyap hutchinsongilfordprogeriasyndromeararecasereport AT vinayshanker hutchinsongilfordprogeriasyndromeararecasereport AT neerajsharma hutchinsongilfordprogeriasyndromeararecasereport |
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