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Hutchinson-Gilford progeria syndrome

Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease in which symptoms of aging are manifested at an early age. In the present report, we describe a 9 months old female child presented with a history of progressive coarsening of skin, failure to thrive and irregular bumps over thigh...

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Autori principali: Zahoor Hussain Daraz, A. B. M. Osman Hayder Mazumder, Shahana A. Rahman
Natura: Artigo
Lingua:Inglês
Pubblicazione: Bangabandhu Sheikh Mujib Medical University 2017-06-01
Serie:Bangabandhu Sheikh Mujib Medical University Journal
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Accesso online:https://www.banglajol.info/index.php/BSMMUJ/article/view/32707
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