Genetic Disease

Over the past 200 years, human life expectancy has approximately doubled. Yet we face soaring worldwide rates of obesity, diabetes, high blood pressure, mental illness, heart disease, and stroke. In his fascinating new book, Dr. Lee Goldman presents a radical explanation: The key protective traits that once ensured our species' survival are now the leading global causes of illness and death.

Simon Dominic Crosier was born on September 7, 2010, in St. Louis, Missouri. He was diagnosed with Trisomy 18, and lived for three memorable months before passing away in December 2010. Despite his disabilities, Simon had a huge impact on all who came into contact with him. The book is about Simon’s short and meaningful life, his family and his wonderful caregivers. But more importantly, this story documents the family’s battle to advocate for their precious son against a sometimes difficult and indifferent medical community. The Crosier family had to overcome challenges put in their ...

For the past six years, Whitney Dafoe has been confined to a bedroom in the back of his parents' home, unable to walk, eat or speak. His diagnosis? The mysterious disease myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) which affects 20 million people around the world who largely suffer in silence because the condition is little known and much misunderstood. Waiting for Superman follows Whitney's father, groundbreaking geneticist Ron, as he uncovers new possibilities for treatments and potentially a cure.

Cystic fibrosis is a life-altering genetic disorder, but with the right knowledge and tools, it can be better understood and managed. The Complete Guide to Cystic Fibrosis provides a clear, comprehensive overview of the disease, making it an essential resource for patients, caregivers, and healthcare professionals.

Che cos'è la sindrome di Down, perché può nascere un bambino con la trisomia 21, e come aiutarlo a crescere fino a farne una persona autonoma e integrata nel mondo della scuola e del lavoro? Il volume, dedicato a genitori, insegnanti, operatori, ripercorre la storia di vita delle persone con sindrome Down e della loro famiglia.

Charlotte Raven had never heard of Huntington's disease when, in her mid-30s, she discovered that her father was suffering from the illness. Life for her and her young family would never be the same again. Patient 1 is her brutally candid account of coming to terms with this inherited neurodegenerative disease, which can manifest at any time in life for people who carry the faulty gene.

19世紀後半にメンデルが発見した遺伝の法則とダーウィンの進化論が出会い、遺伝学は歩み始めた。そして今、人類はゲノム編集の時代を迎えている。遺伝子が握る人類の運命とは？　ピュリッツァー賞受賞の医学者が自らの家系に潜む精神疾患の悲劇を織り交ぜながら、圧倒的なストーリーテリングで紡ぐ遺伝子全史

Health-Wealth for You: 11 Steps to Save Big & Live Healthy teaches individuals and families a series of measurable money-saving tactics that will reduce spending on health care. Dr. Luke, a long-time hospital CEO, simplifies 11 proven steps that Americans can take to reduce health-care spending and improve access to doctors and other providers.

2000年代初頭、人間の全遺伝情報=ヒトゲノムがついに解読された。その後まもなく、山中伸弥らがiPS細胞(人工多能性幹細胞)の作製に成功。そして今、ジェニファー・ダウドナらが開発した新技術「CRISPR-Cas9」により、人類は「ゲノム編集」の時代を迎えている。自らの設計図を望み通りに書き換えられるようになったとき、人間の条件はどう変わるのか? 科学と倫理のせめぎ合いを圧倒的なストーリーテリングで描く傑作。

"The Hate Disease" (1963) is a science fiction short story about the interplanetary medical service, by Murray Leinster. Excerpt: The Med Service people hit strange problems as routine: if they weren't weirdos, they weren't tough enough to merit Med Service attention. Now the essence of a weird problem is that it involves a factor nobody ever thought of before... or the absence of one nobody ever missed... The Med Ship Esclipus Twenty rode in overdrive while her ship's company drank coffee.