Prader-Willi Syndrome: Things You Should Know (Questions and Answers) explains the causes, symptoms, complications, and treatments of this rare genetic condition in a simple question-and-answer format.
Inside, you will learn what Prader-Willi syndrome is, how it develops due to chromosome 15 abnormalities, and why it can affect many parts of the body. The book explains that people with Prader-Willi often experience hyperphagia, low muscle tone, delayed puberty, learning difficulties, behavioral issues, and distinct physical features.
It also covers a wide range of symptoms, including hypogonadism, scoliosis, hypopigmentation, seizures, sleep apnea, obesity, motor and language difficulties, and vision problems such as strabismus and myopia. Behavioral challenges such as stubbornness, skin picking, and anger are also described.
Complications are discussed, including diabetes, high blood pressure, gastric dilation, osteoporosis, heart failure, and respiratory issues. The book also explains diagnostic methods such as genetic testing and outlines treatment approaches, including growth hormone therapy, sex hormone therapy, physical therapy, occupational therapy, speech therapy, diet management, and psychiatric care.
This book is suitable for anyone who wants to understand Prader-Willi syndrome, its effects on the body, and ways it can be managed.