Current diagnosis and management of rare pediatric diseases in China

Author:

Yang Dan1,Ren Xiuzhi2,Lu Yanqin3,Han Jinxiang1

Affiliation:

1. National Health Commission Key Laboratory for Biotech-Drugs, Shandong Province Key Laboratory for Rare & Uncommon Diseases, Biomedical Sciences College, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan, China.

2. Department of Orthopaedic Surgery, The People's Hospital of Wuqing District, Tianjin, China.

3. Department of Endocrinology, The First Hospital Affiliated with Shandong First Medical University, Ji'nan, China.

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Reference59 articles.

1. 1. Chang W. The core of rare diseases is diagnosis and treatment. Minsheng Weekly. 2019; 62-63. (in Chinese)

2. 2. Zhang S. Diagnosis and treatment of rare diseases in China. Clinical Focus. 2019; 34:197-200. (in Chinese)

3. 3. China Pharmaceutical News. Guidelines for the diagnosis and treatment of 121 rare diseases issued for the first time in China. Family Medicine. 2019; 5. (in Chinese)

4. 4. Liu Y, Yang S. Progress in diagnosis and treatment of hypophosphatemic rickets. Chinese J Child Health Care. 2015; 23:486-488. (in Chinese)

5. 5. Quinlan C, Guegan K, Offiah A, Neill RO, Hiorns MP, Ellard S, Bockenhauer D, Hoff WV, Waters AM. Growth in PHEX-associated X-linked hypophosphatemic rickets: The importance of early treatment. Pediatr Nephrol. 2012; 27:581-588.

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