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Diabetes insipidus in childrena pock...

Alter, Craig A.

Diabetes insipidus in childrena pocket guide /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Diabetes insipidus in childrenedited by Craig A. Alter.
Reminder of title:	a pocket guide /
other author:	Alter, Craig A.
Published:	Cham :Springer International Publishing :2021.
Description:	xvii, 193 p. :ill., digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	Diabetes in children.
Online resource:	https://doi.org/10.1007/978-3-030-83248-3
ISBN:	9783030832483$q(electronic bk.)

Diabetes insipidus in childrena pocket guide /
Diabetes insipidus in childrena pocket guide /[electronic resource] :edited by Craig A. Alter. - Cham :Springer International Publishing :2021. - xvii, 193 p. :ill., digital ;24 cm.

Primary Polydipsia -- Diagnosing DI (Water Deprivation) -- MRI Lesions in Diabetes Insipidus -- Central Diabetes Insipidus with Pituitary Stalk Thickening -- Hypophysitis -- Germ Cell Tumors -- The Gist of a Rathke's Cleft Cyst -- Langerhans Cell Histiocytosis and Diabetes Insipidus -- Craniopharyngioma and Diabetes Insipidus -- Diabetes Insipidus after Craniopharyngioma Resection -- Partial Central Diabetes Insipidus Following Endonasal Biopsy -- Septo-optic Dysplasia Spectrum -- Familial Diabetes Insipidus -- Treatment with Thiazides in Infants with Central Diabetes Insipidus -- Absent Thirst and Diabetes Insipidus -- Nephrogenic Diabetes Insipidus.

Utilizing clinical case material of children with diabetes insipidus (DI), this concise, practical pocket guide will provide clinicians with the best real-world strategies to properly diagnose and manage the various manifestations of the disorder they may encounter. It presents a detailed cross-section of pediatric patients, with different etiologies of the disease and possible complications, to provide sensible management scenarios to physicians treating patients with DI. The cases presented include diagnostic strategies and radiological findings for familial and nephrogenic DI as well as DI resulting from hypophysitis, germ cell tumors, Rathkes Cleft Cysts, Langerhans Cell Histiocytosis, craniopharyngiomas, genetic causes, and congenital malformations. Each case focuses on a specific learning objective with clinical pearls, and together these cases represent a comprehensive understanding of children with DI from many aspects. Managing pediatric patients with DI is a threefold challenge of determining the diagnosis, etiology and treatment. Pragmatic and reader-friendly, Diabetes Insipidus in Children is an excellent resource to assist endocrinologists and other clinicians caring for patients with this disease.

ISBN: 9783030832483$q(electronic bk.)

Standard No.: 10.1007/978-3-030-83248-3doiSubjects--Topical Terms:

512230
Diabetes in children.

LC Class. No.: RJ420.D5

Dewey Class. No.: 618.92462

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505 0 $a Primary Polydipsia -- Diagnosing DI (Water Deprivation) -- MRI Lesions in Diabetes Insipidus -- Central Diabetes Insipidus with Pituitary Stalk Thickening -- Hypophysitis -- Germ Cell Tumors -- The Gist of a Rathke's Cleft Cyst -- Langerhans Cell Histiocytosis and Diabetes Insipidus -- Craniopharyngioma and Diabetes Insipidus -- Diabetes Insipidus after Craniopharyngioma Resection -- Partial Central Diabetes Insipidus Following Endonasal Biopsy -- Septo-optic Dysplasia Spectrum -- Familial Diabetes Insipidus -- Treatment with Thiazides in Infants with Central Diabetes Insipidus -- Absent Thirst and Diabetes Insipidus -- Nephrogenic Diabetes Insipidus.
520 $a Utilizing clinical case material of children with diabetes insipidus (DI), this concise, practical pocket guide will provide clinicians with the best real-world strategies to properly diagnose and manage the various manifestations of the disorder they may encounter. It presents a detailed cross-section of pediatric patients, with different etiologies of the disease and possible complications, to provide sensible management scenarios to physicians treating patients with DI. The cases presented include diagnostic strategies and radiological findings for familial and nephrogenic DI as well as DI resulting from hypophysitis, germ cell tumors, Rathkes Cleft Cysts, Langerhans Cell Histiocytosis, craniopharyngiomas, genetic causes, and congenital malformations. Each case focuses on a specific learning objective with clinical pearls, and together these cases represent a comprehensive understanding of children with DI from many aspects. Managing pediatric patients with DI is a threefold challenge of determining the diagnosis, etiology and treatment. Pragmatic and reader-friendly, Diabetes Insipidus in Children is an excellent resource to assist endocrinologists and other clinicians caring for patients with this disease.
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