دورية أكاديمية

Hutchinson-Gilford progeria syndrome

التفاصيل البيبلوغرافية
العنوان: Hutchinson-Gilford progeria syndrome
المؤلفون: Zahoor Hussain Daraz, A. B. M. Osman Hayder Mazumder, Shahana A. Rahman
المصدر: Bangabandhu Sheikh Mujib Medical University Journal, Vol 10, Iss 2 (2017)
بيانات النشر: Bangabandhu Sheikh Mujib Medical University, 2017.
سنة النشر: 2017
المجموعة: LCC:Medicine
مصطلحات موضوعية: Case report, Hutchinson-Gilford progeria syndrome, Medicine
الوصف: 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 thighs, buttocks and lower limbs for the last 7½ months. In the course of time, she developed alopecia, hyperpigmented spots over the abdomen with thickening and a typical facial profile of HGPS including micrognathia, absent ear lobules, prominent eyes, loss of eyelashes, eyebrows and a bluish hue over the nose.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2074-2908
2224-7750
العلاقة: https://www.banglajol.info/index.php/BSMMUJ/article/view/32707Test; https://doaj.org/toc/2074-2908Test; https://doaj.org/toc/2224-7750Test
DOI: 10.3329/bsmmuj.v10i2.32707
الوصول الحر: https://doaj.org/article/d4dea6fbdc634ab998ea4cc01d84dcc8Test
رقم الانضمام: edsdoj.4dea6fbdc634ab998ea4cc01d84dcc8
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20742908
22247750
DOI:10.3329/bsmmuj.v10i2.32707