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Renal tubular acidosis in childrennew insights in diagnosis and treatment /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Renal tubular acidosis in childrenedited by Ricardo Munoz.
Reminder of title:	new insights in diagnosis and treatment /
other author:	Munoz, Ricardo.
Published:	Cham :Springer International Publishing :2022.
Description:	xvi, 154 p. :ill. (some col.), digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	Pediatric nephrologyDiagnosis.
Online resource:	https://doi.org/10.1007/978-3-030-91940-5
ISBN:	9783030919405$q(electronic bk.)

Renal tubular acidosis in childrennew insights in diagnosis and treatment /
Renal tubular acidosis in childrennew insights in diagnosis and treatment /[electronic resource] :edited by Ricardo Munoz. - Cham :Springer International Publishing :2022. - xvi, 154 p. :ill. (some col.), digital ;24 cm.

Systemic Regulation of Acid-Base Metabolism -- Renal Regulation of Acid-Base Metabolism -- Physiology of Renal Potassium Handling -- Genetic Origins of Renal Tubular Acidosis -- History of Renal Tubular Acidosis -- Classification of Renal Tubular Acidosis -- Laboratory Diagnosis of Renal Tubular Acidosis -- Proximal Renal Tubular Acidosis (Type II) -- Distal Renal Tubular Acidosis (Type 1 DRTA) -- Hyperkalemia Renal Tubular Acidosis ( RTA Type IV) -- Renal Tubular Acidosis due to Miscellaneous Etiology.

This book is a compilation of scientific knowledge regarding the clinical entity known as "Renal Tubular Acidosis in Children" (RTA) It contains the information needed to comprehend the intricate mechanisms of acid-base metabolism, electrolyte imbalance, and complications related to renal tubular acidosis in the pediatric age group, since the acid-base physiology and the clinical disorders associated with it in children are quite different from the adult counterpart. The chapters, written by authors, experts in the field, describe systemic and renal physiology, electrolyte alterations, as well as the pathogenesis and chromosomal mutations leading to the development of RTA. The reader will find the latest information on diagnostic tools and learn how to approach diagnosis, avoiding improper treatment, rickets, nephrocalcinosis, and renal failure. In addition, new insights on classification, the clinical presentation of each type of RTA, molecular biology, and transmembrane protein transporters are covered. This work is primarily directed at pediatric nephrologists and pediatricians. Nevertheless, general practitioners, medical students, residents and fellows at different medical training programs, and other health care professionals of nutrition, growth and development, gastroenterology and endocrinology may surely benefit from it.

ISBN: 9783030919405$q(electronic bk.)

Standard No.: 10.1007/978-3-030-91940-5doiSubjects--Topical Terms:

895375
Pediatric nephrology
--Diagnosis.

LC Class. No.: RJ476.K5 / R46 2022

Dewey Class. No.: 618.9261

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505 0 $a Systemic Regulation of Acid-Base Metabolism -- Renal Regulation of Acid-Base Metabolism -- Physiology of Renal Potassium Handling -- Genetic Origins of Renal Tubular Acidosis -- History of Renal Tubular Acidosis -- Classification of Renal Tubular Acidosis -- Laboratory Diagnosis of Renal Tubular Acidosis -- Proximal Renal Tubular Acidosis (Type II) -- Distal Renal Tubular Acidosis (Type 1 DRTA) -- Hyperkalemia Renal Tubular Acidosis ( RTA Type IV) -- Renal Tubular Acidosis due to Miscellaneous Etiology.
520 $a This book is a compilation of scientific knowledge regarding the clinical entity known as "Renal Tubular Acidosis in Children" (RTA) It contains the information needed to comprehend the intricate mechanisms of acid-base metabolism, electrolyte imbalance, and complications related to renal tubular acidosis in the pediatric age group, since the acid-base physiology and the clinical disorders associated with it in children are quite different from the adult counterpart. The chapters, written by authors, experts in the field, describe systemic and renal physiology, electrolyte alterations, as well as the pathogenesis and chromosomal mutations leading to the development of RTA. The reader will find the latest information on diagnostic tools and learn how to approach diagnosis, avoiding improper treatment, rickets, nephrocalcinosis, and renal failure. In addition, new insights on classification, the clinical presentation of each type of RTA, molecular biology, and transmembrane protein transporters are covered. This work is primarily directed at pediatric nephrologists and pediatricians. Nevertheless, general practitioners, medical students, residents and fellows at different medical training programs, and other health care professionals of nutrition, growth and development, gastroenterology and endocrinology may surely benefit from it.
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