在一个年轻的亚洲儿童中,双边肢体干细胞缺乏与色素的Xeroderma pigmentum
Bharat Gurnani1, Kirandeep Kaur2
1Cataract, Cornea, External Disease, Trauma, Ocular Surface and Refractive Services Sadguru Netra Chikitsalya, Shri Sadguru Seva Sangh Trust Chitrakoot Madhya Pradesh India.
Clinical case reports
|August 2, 2023
概括
Xeroderma pigmentosum (XP) 很少会导致双边四肢干细胞缺乏症 (LSCD). 早期检测和管理对于预防眼部并发症的XP患者的视力损失至关重要.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 遗传学 是一个
- 皮肤病学 皮肤病学
背景情况:
- Xeroderma pigmentosum (XP) 是一种罕见的自体逆向性疾病,其特征是缺陷的DNA修复机制.
- 眼部表现在XP中很常见,但肢体干细胞缺乏 (LSCD) 是一个不常见的并发症.
- 早期诊断和管理对于预防严重的眼部后果至关重要.
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