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By Eugene Toy, Visit Amazon's Robert Yetman Page, search results, Learn about Author Central, Robert Yetman, , Rebecca Girardet, Mark Hormann, Sheela Lahoti, Margaret McNeese, Mark Jason Sanders
Real-Life circumstances for the Pediatrics clerkship and the shelf-exam you would like publicity to high-yield instances to excel at the pediatrics clerkship and at the shelf-exam. Case records: Pediatrics provides 60 real-life instances that illustrate crucial ideas in pediatrics. each one case contains a entire dialogue, medical pearls, references, definitions of keyword phrases, and USMLE-style assessment questions. With the program, you will research within the context of genuine sufferers, instead of in simple terms memorize facts.p> positive factors: 60 high-yield pediatrics instances, every one with USMLE-style questions medical pearls spotlight key options Primer on the best way to strategy scientific difficulties and imagine like a physician confirmed studying approach maximizes your shelf-exam ratings
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Extra info for Case Files Pediatrics, Third Edition (LANGE Case Files)
These children can have a syndrome (a constellation of features from a common cause; ie, DS features caused by extra chromosome 21 material); an association (two or more features of unknown cause occurring together more commonly than expected; ie, VATER [Vertebral problems, Anal anomalies, Trachea problems, Esophageal abnormalities, and Radius or renal anomalies]), or a sequence (a single defect that leads to subsequent abnormalities; ie, Potter disease’s lack of normal infant kidney function, causing reduced urine output, oligohydramnios, and constraint deformities; common facial features include wide-set eyes, flattened palpebral fissures, prominent epicanthus, flattened nasal bridge, mandibular micrognathia, and large, low-set, cartilage-deficient ears).
Patients with renal tubular acidosis, a common cause of organic failure to thrive, can have proximal tubule defects (type 2) caused by impaired tubular bicarbonate reabsorption or distal tubule defects (type 1) caused by impaired hydrogen ion secretion. Type 4 is also a distal tubule problem associated with impaired ammoniagenesis. REFERENCES Bauchner H. Failure to thrive. In: Kleigman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th ed. Philadelphia, PA: WB Saunders; 2007:184-187.
Findings include characteristic facies and velocardiofacial defects such as ventricular septal defect and tetralogy of Fallot. Thymic or parathyroid dysgenesis can occur, accompanied by hypocalcemia and seizures. Developmental and speech delay are common in older patients. 50 CASE FILES: Pe d i a t r i c s Clinical Pearls ➤ Primary immunodeficiency is an inheritable disorder characterized by weakened immunity and recurring, serious infection early in life. ➤ A variety of illnesses can provoke secondary immunodeficiency; malignancy, malnutrition, hepatic disease, and human immunodeficiency virus (HIV) infection are known to adversely influence both humoral and cellular immunity.