Hunter syndrome with hyperthyroidism: a 16 month follow-up reprt

• 主要な著者: Din Alfina (著者), Endy Paryanto Prawirohartono (著者), Roni Naning (著者), Neti Nurani (著者)
• フォーマット: 図書
• 出版事項: Indonesian Pediatric Society Publishing House, 2018-12-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Mucopolysaccharidosis (MPS) is a rare genetic disorder caused by a deficiency in the activity of lysosomal enzymes required for glycosaminoglycan (GAG) degradation. An accumulation of GAG in many organs results in progressive cellular damage, and clinically results in joint stiffness, airway and car...