Rare diseases in children: towards better and fairer treatmentdoi:10.1016/S0140-6736(14)61194-6The LancetThe Lancet
The Oxford Handbook of Children's Literature . Oxford/NY: Oxford... D Stevenson - 《Lion & the Unicorn》 被引量: 10发表: 2011年 Orphan diseases: which ones do we adopt? If diseases that affect so many people remain neglected, how strong is the case for investing in research into rare...
Preoperative preparation of children with respiratory diseases Children have a number of anatomical and functional characteristics of the respiratory system as adults do. Perioperative respiratory complications are more common in children's age. In the presence of acute upper respiratory tract infec... Dr...
However, many patients and their families face an uphill battle, as NF is yet to be officially recognized as a rare disease in China or included in the country’s list of rare diseases. That’s why the center is using ...
Parents in Korea and other Asian countries are unusually concerned about their children's height. That is partly because Asians tend to be shorter than people in the West. Still, this interest in height has given rise to the academic term "heightism" in
Rare Diseases (RDs) in adolescents are characterized by low frequency and clinical heterogeneity, are chronic and deliberating and demand a multidisciplinary approach as well as costly and specialized treatments. Comprehending patients’ and parents’ needs through a mixed systematic review is essential fo...
Children affecting with rare diseases are Rare Pediatric diseases, there are various causes forpediatric diseasessome of the rare pediatric diseases are, Congenital Heart Defects, Eisenmenger Syndrome, Kawasaki Disease. Related Journals to Rare Pediatric diseases ...
Since November 2022, experts from Shanghai Children's Medical Center have come to Guizhou to carry out diagnosis, treatment, and operations for children with complex and baffling diseases, including rare diseases. In March, Guizhou Hospital of Shanghai Children's Medical Center will be put into ...
Invisible patients in rare diseases: parental experiences with the healthcare and social services for children with rare diseases. A mixed method study Article Open access 18 June 2024 Living with a rare disease - experiences and needs in pediatric patients and their parents Article Open access...
Duchenne muscular dystrophy (DMD) is a clinically common X-linked recessive myopathy, which is caused by mutation of the gene encoding dystrophin on chromosome Xp21. The onset of heart injury in children with DMD is inconspicuous, and the prognosis is po