Offering exceptional full color diagrams and clinical images, Langman’s Medical Embryology, 13e helps medical, nursing, and health professions students develop a basic understanding of embryology and its clinical relevance. Concise chapter summaries, captivating clinical correlates boxes, clinical problems, and a clear, concise writing style make the subject matter accessible to students and relevant to instructors. And then nothing turned itself inside-out rar.
The new edition is enhanced by over 100 new and updated illustrations, additional clinical images and photos of early embryologic development, and an expanded chapter on the cardiovascular system. Clinical Correlates boxes illustrated by cases and images cover birth defects, developmental abnormalities, and other clinical phenomena. More than 400 illustrations—including full-color line drawings, scanning electron micrographs, and clinical images—clarify key aspects of embryonic development.
Basic genetic molecular biology principles are highlighted throughout the text to link embryology to other critical specialties. Chapter Overview figures provide a visually compelling introduction to each chapter. Problems to Solve (with detailed answers at the back of the book) help you assess your understanding. An expanded glossary defines key terms and concepts. Online learning resources for students include an interactive question bank and animations.
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Congenital anomalies concerning the kidneys and urinary tract represent a heterogeneous group of defects and the main cause of renal failure during childhood. Kidney hypoplasia is one such defect; it is defined in clinical practice as a kidney which is significantly shorter than normal but retains a normal shape and some of its function.
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Bilateral congenital kidney hypoplasia (BCKH) is 7 times less more frequent than unilateral hypoplasia, thus being one of the rarest anomalies of the kidney and urinary tract. The presence of BCKH in more than one family member is even rarer. This article deals with two male brothers having BCKH diagnosed through ultrasonography of the kidneys and urinary tract.
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A postnatal diagnosis was made for both of them; the younger brother received his diagnosis when he was 4 years old after being studied for the persistence of low height for his age and the older brother received his at 8 years of age after decreased renal function was revealed during hospitalisation. Ultrasonography study showed reduced size for both kidneys in both cases, according to Hodson's index. This article discusses aspects concerning this congenital anomaly and highlights this disorder's importance in some clinical scenarios. It is hoped that this information may be of use during the initial approach to the family of a BCRH patient.
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