دورية أكاديمية
Hutchinson-Gilford progeria syndrome
العنوان: | Hutchinson-Gilford progeria syndrome |
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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 |
تدمد: | 20742908 22247750 |
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DOI: | 10.3329/bsmmuj.v10i2.32707 |