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Titlebook: Medical and Surgical Complications of Sickle Cell Anemia; Ahmed Al-Salem Book 2016 Springer International Publishing Switzerland 2016 Acut

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发表于 2025-3-21 17:37:33 | 显示全部楼层 |阅读模式
书目名称Medical and Surgical Complications of Sickle Cell Anemia
编辑Ahmed Al-Salem
视频video
概述Aids in the diagnosis and management of a wide range of complications.Presented in a bullet point format that makes the book an ideal quick reference.Includes numerous high-quality illustrations
图书封面Titlebook: Medical and Surgical Complications of Sickle Cell Anemia;  Ahmed Al-Salem Book 2016 Springer International Publishing Switzerland 2016 Acut
描述.This book is a wide-ranging guide to the diagnosis and management of the numerous medical and surgical complications that may arise in patients with sickle cell anemia. After introductory chapters on the genetics, pathophysiology, clinical features, and variants of sickle cell anemia, the complications observed in different parts of the body are addressed in a series of well-illustrated chapters. The coverage includes splenic, hepatobiliary, musculoskeletal, gastrointestinal, ophthalmological, cardio- and cerebrovascular, and renal complications, as well as acute chest syndrome, leg ulcers, hand and foot syndrome, acute appendicitis, and priapism. Treatment-oriented chapters consider perioperative management, blood transfusion therapy, hydroxyurea treatment, hematopoietic stem cell transplantation, and emerging strategies. The book is clearly written in a distinctive bullet point format for ease of reference and emphasizes especially aspects of practical significance. It will be ofvalue for hematologists, general surgeons, internists, pediatricians, pediatric surgeons, fellows, residents, medical students, and nurses. .
出版日期Book 2016
关键词Acute Chest Syndrome; Cholelithiasis; Medical Complications; Sickle Cell Anemia; Splenic Complications; S
版次1
doihttps://doi.org/10.1007/978-3-319-24762-5
isbn_softcover978-3-319-79673-4
isbn_ebook978-3-319-24762-5
copyrightSpringer International Publishing Switzerland 2016
The information of publication is updating

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发表于 2025-3-21 22:24:46 | 显示全部楼层
Book 2016sickle cell anemia. After introductory chapters on the genetics, pathophysiology, clinical features, and variants of sickle cell anemia, the complications observed in different parts of the body are addressed in a series of well-illustrated chapters. The coverage includes splenic, hepatobiliary, mus
发表于 2025-3-22 04:08:33 | 显示全部楼层
发表于 2025-3-22 06:11:42 | 显示全部楼层
Genetics and Pathophysiology of Sickle Cell Anemia,The normal hemoglobin is made up of two parts, heme and protein. The protein is made up of four polypeptide chains (Fig. 2.1):
发表于 2025-3-22 12:03:29 | 显示全部楼层
Variants of Sickle Cell Anemia,The normal hemoglobin is made up of two parts (Fig. 3.1):
发表于 2025-3-22 16:03:55 | 显示全部楼层
The Spleen and Sickle Cell Anemia,The word spleen comes from the Greek σπλήν (.) and is the idiomatic equivalent of the heart in English, i.e., to be good-spleened (εὔσπλαγχνος, .) means to be good-hearted or compassionate.
发表于 2025-3-22 19:23:15 | 显示全部楼层
发表于 2025-3-23 00:40:16 | 显示全部楼层
The Acute Chest Syndrome in Sickle Cell Anemia,Acute chest syndrome (ACS) is defined as a new infiltrate on chest X-ray that is associated with one or more of the following symptoms:
发表于 2025-3-23 04:43:58 | 显示全部楼层
Musculoskeletal Manifestations of Sickle Cell Anemia,One of the common manifestations of sickle cell anemia is vaso-occlusive crises which affect virtually all patients with sickle cell anemia.
发表于 2025-3-23 06:21:05 | 显示全部楼层
Gastrointestinal Complications of Sickle Cell Anemia,Sickle cell anemia is one of the most common inherited hemoglobinopathies worldwide.
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