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E-grāmata: Brook's Clinical Pediatric Endocrinology, 7th Edition 7th Edition [Wiley Online]

Edited by (University College and The Middlesex Hospital, London), Edited by (UCL Institute of Child Health, University College London, UK)
  • Formāts: 816 pages
  • Izdošanas datums: 01-Nov-2019
  • Izdevniecība: Wiley-Blackwell
  • ISBN-10: 1119152712
  • ISBN-13: 9781119152712
Citas grāmatas par šo tēmu:
  • Wiley Online
  • Cena: 308,56 €*
  • * this price gives unlimited concurrent access for unlimited time
  • Formāts: 816 pages
  • Izdošanas datums: 01-Nov-2019
  • Izdevniecība: Wiley-Blackwell
  • ISBN-10: 1119152712
  • ISBN-13: 9781119152712
Citas grāmatas par šo tēmu:
"The seventh edition of Brook's Clinical Pediatric Endocrinology has been compiled by an experienced editorial team and internationally renowned contributors; it presents basic science and clinical management of endocrine disorders for all involved in the care of children and adolescents. It provides treatments for a variety of hormonal diseases, including diabetes and hypoglycaemia, growth problems, thyroid disease and disorders of puberty, sexual differentiation, calcium metabolism, steroid metabolism and hypopituitarism"--Provided by publisher.

The seventh edition of Brook's Clinical Pediatric Endocrinology has been compiled by an experienced editorial team and internationally renowned contributors; it presents basic science and clinical management of endocrine disorders for all involved in the care of children and adolescents. It provides treatments for a variety of hormonal diseases, including diabetes and hypoglycaemia, growth problems, thyroid disease and disorders of puberty, sexual differentiation, calcium metabolism, steroid metabolism and hypopituitarism.

List of Contributors xix
Preface xxiii
About the Companion Website xxv
1 Genetics and Genomics 1(30)
Anu Bashamboo
Ken McElreavey
Introduction
1(1)
Basic Concepts in Human Genetics and Genomics
1(3)
Genes and Chromosomes
1(3)
Regulation of Gene Expression
4(1)
RNA Editing
4(1)
Classes of RNA Molecules and their Functions
4(3)
MicroRNAs, Small Interfering RNAs, and Piwi-interacting RNAs
5(1)
LncRNAs
6(1)
Other Small ncRNA Classes
7(1)
Gene Mutations and Inheritance
7(5)
Classes of Gene Mutations
7(1)
Patient and Family History
8(1)
Mendelian Inheritance Patterns
8(1)
Non-Mendelian Inheritance Patterns
9(1)
Common Disorders with Complex Inheritance Patterns
10(1)
Uniparental Disomy
11(1)
Penetrance and Expressivity
11(1)
Human Populations and Genetic Variation
12(2)
Overview of Human Genetic Variation
12(1)
Allele Frequencies Differ in Different Populations
12(1)
Copy Number Variation (CNV)
13(1)
Epigenetics
14(1)
Epigenetic Mechanisms
14(1)
Genomic Imprinting
14(1)
Transgenerational and Multigenerational Epigenetic Inheritance
15(1)
Advances in Genomic Analysis
15(4)
Familial Linkage Analysis and GWAS Studies
15(1)
Advances in Nucleic Acid Sequencing
16(1)
NGS Protocols
17(1)
Whole Genome (WGS) and Whole Exome Sequencing (WES)
17(2)
Establishing Variant Causality
19(5)
Dissecting Pathogenic from Non-Pathogenic Variants
19(3)
Genome Editing as a Powerful Tool for Establishing Causality
22(2)
The Age of Precision Medicine
24(1)
Clinical Guidelines
24(1)
Acknowledgments
25(1)
Glossary of Terms
25(4)
Further Reading
29(2)
2 Measuring Hormones 31(16)
Gerhard Binder
Introduction
31(1)
Hormone Assays
31(2)
Assay Validity
33(3)
Technical Pitfalls When Measuring Hormones
36(2)
Clinical Assay Validity
38(4)
Stimulation Tests, Suppression Tests and Profiles
42(2)
Optimal Clinical Use of Hormone Tests
44(1)
Acknowledgements
44(1)
References
44(3)
3 Fetal Endocrinology 47(58)
Harshini Katugampola
Evelien F. Gevers
Mehul T. Dattani
Introduction
48(1)
Transplacental Passage of Hormones
48(2)
Development of Fetal Endocrine Systems
50(32)
Pituitary Development
50(5)
Adrenal Development
55(7)
Thyroid Development
62(4)
Gonadal Development
66(3)
Disorders of Sex Development (see
Chapter 4)
69(1)
Development of the Fetal Autonomic Nervous System
69(2)
Development of the Endocrine Pancreas
71(2)
Development of Pancreatic Endocrine Function
73(2)
Development of the Parathyroid/Calcitonin System
75(3)
Endocrine Regulation of Fetal Growth
78(4)
Neutralization of Hormone Activity in the Fetus
82(2)
Limitation of Hormone Secretion
82(1)
Production of Inactive Hormone Metabolites
83(1)
Delayed Expression or Neutralization of Receptor Response
83(1)
Plasticity of Fetal Endocrine Systems
84(1)
Fetal Adaptations for Transition to Extrauterine Life
85(4)
Cortisol
86(1)
Catecholamines
87(1)
Thermogenesis
87(1)
Calcium Homeostasis
87(1)
Glucose Homeostasis
88(1)
Other Endocrine Adaptations
88(1)
Frontiers in Fetal and Neonatal Endocrinology
89(1)
References
90(15)
4 Disorders of Sex Development 105(28)
Martine Cools
Birgit Kohler
Normal Sex Development
105(1)
Terminology
106(1)
Causes of DSD
107(1)
Impaired Gonadal Development
108(5)
XY Individuals
108(3)
XX individuals
111(1)
Numerical Abnormalities of the Sex Chromosomes
112(1)
Disturbances of Testicular Hormone Production or Action
113(3)
Impaired Biosynthesis
113(1)
Impaired Testosterone Action
114(2)
Virilization of an XX Individual
116(2)
Management of DSD
118(4)
Initial Evaluation and Diagnostic Approach
118(1)
Examination
119(1)
Hormonal Workup
119(2)
Genetic Tests
121(1)
Sex Assignment, Gender Development, Early Genital Surgery and Disclosure of the Condition
121(1)
Clinical Management
122(4)
Gonadal Tumour Risk and Indications for Gonadectomy
123(1)
Information and Support for Parents Having a Baby with DSD
124(1)
Information and Support for Children and Adolescents
124(1)
Transition
124(1)
Adult Outcome
125(1)
Other Examples of XY DSD
126(1)
Hypospadias
126(1)
Cryptorchidism
126(1)
Persistent Mullerian Duct Syndrome
126(1)
Future Perspectives
127(1)
References
127(4)
Weblinks
131(2)
5 Disorders of Hypothalamo-Pituitary Axis 133(66)
Hoong-Wei Gan
Kyriaki-Sandy Alatzoglou
Mehul T. Dattani
Introduction
133(1)
The Hypothalamo-Pituitary Neuroendocrine Axis
134(1)
Hypothalamo-Pituitary Development
134(10)
Hypothalamo-Pituitary Organogenesis
135(1)
Cell Differentiation, Organization and Plasticity in the Anterior Pituitary
136(1)
Early Developmental Genes and Transcription Factors
137(6)
Terminal Cell Differentiation
143(1)
Congenital Disorders of Hypothalamo-Pituitary Development
144(11)
Combined Pituitary Hormone Deficiencies (CPHD)
144(8)
Isolated Pituitary Hormone Deficiencies
152(3)
Acquired Disorders of Hypothalamo-Pituitary Dysfunction
155(17)
Central Nervous System (CNS) Tumours
155(11)
Infiltrative and Inflammatory Disorders
166(2)
Traumatic Brain Injury
168(1)
CNS Infection
169(1)
Haemochromatosis
170(1)
Psychosocial Deprivation
171(1)
Investigation of Hypopituitarism
172(1)
Management of Hypopituitarism
173(1)
Conclusion
174(1)
References
174(25)
6 Disorders of Growth 199(36)
P.G. Murray
P.E. Clayton
Normal Growth
200(5)
Physiology of Growth
201(4)
Short Stature
205(6)
Aetiology of Growth Impairment
205(1)
Growth Hormone Deficiency
205(1)
Biochemical Evaluation of Suspected GH Deficiency
206(2)
Neuroimaging
208(1)
Genetic Studies
208(1)
Management of Growth Hormone Deficiency
208(2)
Safety of Growth Hormone Treatment
210(1)
Reassessment of the GH-IGF Axis at End of Growth
210(1)
Monogenic Disorders Causing Growth Hormone Deficiency
211(1)
Acquired GH Deficiency
211(2)
Tumours Affecting the Hypothalamo-Pituitary Axis
211(1)
Radiotherapy
212(1)
Langerhans Cell Histiocytosis
213(1)
Trauma
213(1)
Hypophysitis
213(1)
Disorders of GH Action and GH Sensitivity (Primary IGF-I Deficiency)
213(3)
Bioinactive GH
213(1)
Laron Syndrome
214(1)
STAT5B Deficiency
214(1)
Acid-Labile Subunit (ALS) Deficiency
214(1)
IGF-I Gene Deletions and Bioinactive IGF-I
215(1)
Recombinant Human IGF-I Therapy
215(1)
Disorders of IGF-I Resistance
216(1)
Growth Disorders not Related to the GH-IGF Axis
216(3)
The Short Small-for-Gestational-Age Child
216(1)
Management of Child Born SGA
217(1)
Turner Syndrome
217(2)
Syndromes Associated With Short Stature
219(6)
Prader-Willi Syndrome
219(1)
Noonan Syndrome and Associated Disorders
220(1)
Primordial Growth Disorders
220(1)
Silver-Russell Syndrome
220(3)
3-M Syndrome
223(1)
Mulibrey Nanism
223(1)
SHORT Syndrome
223(1)
Floating-Harbor Syndrome
223(1)
IMAG e Syndrome
224(1)
Bloom Syndrome
224(1)
Microcephalic Osteodysplastic Primordial Dwarfism Type II
224(1)
Seckel Syndrome
224(1)
Meier-Gorlin Syndrome
224(1)
Nijmegen Breakage Syndrome
224(1)
Fanconi Anaemia
224(1)
Idiopathic Short Stature
225(2)
Treatment of ISS
226(1)
Skeletal Dysplasias
227(2)
Skeletal Dysplasia Classification
227(1)
Achondroplasia
228(1)
Hypochondroplasia
228(1)
Leri-Weill Dyschondrosteosis and SHOX Deficiency
229(1)
Tall Stature
229(4)
Familial Tall Stature, Constitutional Tall Stature and Obesity
230(1)
Precocious Puberty
230(1)
GH Excess
230(1)
Syndromes Associated with Tall Stature
231(1)
Management of Tall Stature
232(1)
References
233(2)
7 Puberty and Its Disorders 235(54)
Sasha R. Howard
Nicolas de Roux
Juliane Leger
Jean-Claude Carel
Leo Dunkel
Normal Puberty
235(21)
Introduction
235(1)
Physical Changes that Occur During Puberty
236(3)
Timing of Puberty and Relationship with Linear Growth
239(6)
The Hypothalamic-Pituitary-Gonadal Axis
245(8)
The Reactivation of the Gonadotropic Axis at Puberty
253(3)
Precocious Puberty
256(9)
Introduction
256(1)
Aetiologies of Premature Sexual Development
256(3)
Consequences of Precocious Puberty
259(1)
Evaluation of the Child with Premature Sexual Development
259(5)
Management
264(1)
Delayed Puberty
265(18)
Definition
265(1)
Differential Diagnosis
265(10)
Assessment
275(3)
Management
278(5)
Conclusions
283(1)
References
284(5)
8 The Thyroid Gland 289(46)
Catherine Peters
Nadia Schoenmakers
Section 1: Development of the Thyroid Axis
289(12)
Thyroid Gland Development
289(1)
Molecular Control of Thyroid Development
290(1)
Thyroid Hormone Biosynthesis
290(2)
The Hypothalamic-Pituitary-Thyroid Axis
292(1)
Negative Regulation of Thyroid Hormone Synthesis
292(1)
Thyroid Hormone Transport
293(1)
Thyroid Hormone Transport Proteins
293(1)
Thyroid Hormone Metabolism
293(1)
Thyroid Hormone Action
294(2)
Positive Regulation of Genes by Thyroid Hormone
296(1)
Negative Regulation of Genes by Thyroid Hormone
296(1)
Thyroid Hormone Receptor Function
296(1)
Thyroid Hormone Effects on Target Tissues
296(1)
Thyroid Hormone Effects on the Gut
297(1)
Maturation of Thyroid Hormone Development
298(3)
Section 2: Clinical Thyroid Disorders
301(14)
Congenital Hypothyroidism
301(7)
Prematurity
308(1)
Drugs/Iatrogenic
308(1)
Fetal and Neonatal Goitre
308(1)
Congenital Hyperthyroidism
308(1)
TSH Receptor Mutation
309(1)
McCune-Albright Syndrome
309(1)
Acquired Thyroid Disorders
309(1)
Hashimoto's Thyroiditis
310(1)
Graves' Disease
311(2)
Thyroid Storm
313(1)
Thyrotoxic Periodic Paralysis
313(1)
Other Forms of Thyroiditis
314(1)
Subacute (De Quervain's) Thyroiditis
314(1)
Euthyroid Goitre
314(1)
Thyroid Nodule
314(1)
Iodine Status
314(1)
Section 3: Diagnostic Pitfalls
315(5)
Normal Thyroid Hormone with Elevated TSH
315(1)
Reduced Thyroid Hormones Without TSH Elevation
315(1)
Elevated Thyroid Hormones and Unsuppressed TSH
315(2)
Defective TH Action - Resistance to Thyroid Hormone (RTH)
317(1)
Defective TH Metabolism - SECISBP2
318(1)
Defective Thyroid Hormone Transport - MCT8
319(1)
Familial Dysalbuminaemic Hyperthyroxinaemia (FDH)
319(1)
References
320(14)
Weblinks
334(1)
9 The Adrenal Cortex and Its Disorders 335(74)
Claire R. Hughes
Elim Man
John C. Achermann
Introduction
335(1)
Development, Function and Regulation of the Adrenal Gland
336(17)
History of Adrenal Medicine
336(1)
Development and Anatomy of the Adrenal Gland
336(3)
Steroidogenesis
339(7)
Dynamic Regulation of Steroidogenesis
346(4)
Steroid Hormone Actions
350(3)
Adrenal Insufficiency (AI)
353(40)
Overview of AI
353(2)
Presentation of AI
355(3)
Diagnosing AI and its Causes
358(9)
Treatment of AI
367(3)
Secondary AI
370(2)
Causes of Primary AI (Excluding CAH)
372(9)
Congenital Adrenal Hyperplasia (CAH)
381(12)
Adrenal Excess
393(8)
Glucocorticoid Excess (Cushing Syndrome)
393(6)
Mineralocorticoid Excess
399(1)
Androgen Excess
400(1)
Education, Support and Long-Term Care
401(8)
Education
401(2)
Support Organizations
403(1)
Transition and Long-Term Care
404(1)
References
405(4)
10 The Parathyroid and Disorders of Calcium and Bone Metabolism 409(72)
Jeremy Allgrove
Moira Cheung
Introduction
409(1)
Physiology of Calcium and Bone Metabolism
409(12)
Cations and Anions
409(4)
Hormones and Other Calciotropic Agents
413(8)
Physiology of Bone Metabolism
421(4)
Bone Matrix
422(1)
Bone Mineral
423(1)
Bone Cells
423(2)
Interactions between Calciotropic Agents
425(1)
Fetal and Neonatal Calcium Metabolism
425(1)
Post-Neonatal Calcium, Phosphate and Magnesium Metabolism and the Calcium Cascade
426(1)
Investigation of Mineral Disorders
426(1)
Clinical Conditions
426(41)
Bone Disease of Prematurity (BDP)
426(2)
Hypocalcaemia
428(18)
Hypercalcaemia
446(8)
Disorders of Bone Metabolism
454(1)
Investigation of Bone Metabolic Disorders
454(1)
Disorders of Bone Matrix Accompanied by Low Bone Density
455(4)
Diseases Characterized by Increased Bone Density
459(5)
Inherited Inflammatory Diseases of Bone
464(1)
Disorders of Phosphate Metabolism
465(2)
Drugs Used in the Treatment of Disorders of Calcium and Bone Metabolism
467(3)
Vitamin D
467(1)
Vitamin D Metabolites
467(1)
Teriparatide (Forsteo®)
468(1)
The Bisphosphonates
468(1)
Denosumab
469(1)
FGF23 Monoclonal Antibody (Burosumab [ KRN23])
469(1)
Corticosteroids
469(1)
Loop diuretics
469(1)
Acetazolamide
469(1)
Calcitonin
470(1)
Phosphate Supplements
470(1)
Phosphate Binders
470(1)
Cinacalcet (Mimpara®)
470(1)
Magnesium Supplements
470(1)
Cathepsin K Inhibitor
470(1)
Anti-Sclerostin Antibody
470(1)
Recombinant Human Non-Specific Alkaline Phosphatase
470(1)
Palovarotene
470(1)
Sodium Thiosulphate
470(1)
Summary
470(2)
References
472(7)
Weblinks
479(2)
11 Polyglandular Autoimmune Syndromes 481(26)
Catherine J. Owen
Mario Abinun
Simon H.S. Pearce
Tim D. Cheetham
Introduction
481(2)
Autoimmune Polyendocrinopathy Syndrome Type 1 (APS1)
483(11)
Definition
483(1)
Clinical Features and Course
483(1)
Cardinal Manifestations
483(2)
Minor Manifestations
485(1)
Other Manifestations
486(1)
Genetics
487(2)
Autoantibodies and Pathogenesis
489(1)
Diagnosis of APS1
490(1)
Follow-up
491(1)
Treatment
492(2)
Prognosis
494(1)
Summary
494(1)
Autoimmune Polyendocrinopathy Syndrome Type 2 and Associated Disorders
494(5)
Definitions
494(1)
APS2
494(2)
APS3
496(1)
Genetics
496(1)
Autoantibodies and Pathogenesis
497(1)
Diagnosis and Follow-up
498(1)
Management
498(1)
Prognosis
499(1)
Summary
499(1)
Other Single Gene Disorders Associated with Immune Dysregulation and Autoimmune Endocrinopathies
499(3)
Conclusion
502(1)
References
502(5)
12 Endocrine Neoplasia 507(26)
Constantine A. Stratakis
Emmanouil Saloustros
Thyroid Neoplasia: Nodules and Cancer
507(4)
Epidemiology
507(1)
Pathogenesis
508(1)
Clinical Presentation and Diagnostic Evaluation
508(1)
Management
509(2)
Paragangliomas and Phaeochromocytomas
511(10)
Epidemiology
511(1)
Pathology
511(1)
Pathogenesis
511(1)
Genetic Syndromes Associated with PHEOs/PGLs
512(4)
Clinical Presentation
516(1)
Diagnosis
516(2)
Treatment
518(3)
Adrenocortical Cancers
521(3)
Epidemiology
521(1)
Pathogenesis
521(1)
Clinical Presentation
522(1)
Diagnosis
523(1)
Treatment
523(1)
Tumours of the Ovary
524(4)
Ovarian Germ Cell Tumours (GCTs)
524(1)
Ovarian Sex Cord Stromal Tumours (SCSTs)
525(3)
Tumours of the Testes
528(2)
Testicular Germ Cell Tumours (GCTs)
528(1)
Testicular Stromal Cell Tumours (SCTs)
529(1)
References
530(3)
13 Endocrine Late Effects of Cancer Treatments 533(20)
Wassim Chemaitilly
Melissa M. Hudson
Prevalence and Risk Factors for Endocrine Late Effects
538(8)
Survivors of Childhood Central Nervous System (CNS) Tumours
538(3)
Survivors Treated with Haematopoietic Stem Cell Transplantation (HSCT) for Haematological Malignancies
541(2)
Endocrine Late Effects in Survivors of Non-HSCT Requiring Childhood Leukaemia
543(1)
Endocrine Late Effects in Survivors of Childhood Hodgkin's Lymphoma (HL)
544(1)
Endocrine Late Effects in Survivors of Childhood Malignant Extra-Cranial Solid Tumours
545(1)
Diagnosis and Management of Common Endocrine Late Effects
546(4)
Disorders of the Hypothalamo-Pituitary Axis
546(1)
Disorders of the Thyroid
547(1)
Disorders of the Gonads
548(1)
Bone Mineral Density Deficit
548(1)
Overweight, Obesity and Glucose Intolerance
548(1)
Preparing for the Transition to the Adult Care Setting
549(1)
Endocrine Complications and Novel Cancer Therapies
549(1)
Summary
550(1)
References
550(2)
Weblinks
552(1)
14 Disorders of Water Balance 553(30)
Natascia Di Iorgi
Flavia Napoli
Giovanni Morana
Mohamad Maghnie
Regulation of Water Balance
554(4)
Anatomy of the Hypothalamic-Posterior Pituitary Axis
554(1)
Neurons, Periphery and Regulation of Thirst
554(1)
Vasopressin Biosynthesis
555(1)
Physiology of Water Homeostasis
556(1)
Regulation of Vasopressin Secretion
557(1)
Diabetes Insipidus (DI)
558(14)
Definition of DI
558(1)
Epidemiology
558(1)
Central Diabetes Insipidus
559(1)
Genetic Forms of Central Diabetes Insipidus
559(2)
Acquired Forms of Idiopathic Central Diabetes Insipidus (CDI)
561(3)
Diagnosis of Central Diabetes Insipidus
564(2)
Imaging Findings in CDI
566(5)
Follow-up and Long-Term Outcomes
571(1)
Central Diabetes Insipidus and Adipsia
572(1)
Primary Polydipsia
572(1)
Nephrogenic Diabetes Insipidus
573(1)
The Syndrome of Inappropriate Antidiuretic Hormone Secretion
573(1)
Management of Central Diabetes Insipidus
573(1)
Treatment of Nephrogenic Diabetes Insipidus
574(1)
Treatment of Inappropriate Antidiuretic Hormone Secretion
574(1)
Challenges
575(1)
Conclusions
575(1)
Clinical Guidelines
575(1)
References
576(7)
15 Diabetes Mellitus 583(88)
G.R. Ambler
F.J. Cameron
K. Joshi
D.K. Wherrett
Type 1 Diabetes
583(43)
Epidemiology
583(2)
Pathophysiology
585(5)
Preventive Interventions
590(3)
Diagnosis
593(1)
Management and Therapies
594(21)
Acute Complications
615(7)
Chronic Complications
622(3)
Prognosis
625(1)
Type 2 Diabetes
626(11)
Epidemiology
626(1)
Pathophysiology
626(6)
Preventive Interventions
632(1)
Diagnosis
632(1)
Management and Therapies
633(3)
Acute Complications
636(1)
Chronic Complications
636(1)
Prognosis
637(1)
Cystic Fibrosis-Related Diabetes
637(2)
Incidence
638(1)
Diagnosis
638(1)
Management and Therapies
638(1)
Prognosis
639(1)
Other Dysglycaemia in Cystic Fibrosis
639(1)
Monogenic Forms of Diabetes
639(8)
Maturity Onset Diabetes of The Young (MODY)
639(3)
Neonatal Diabetes Mellitus (NDM)
642(1)
Transient Neonatal Diabetes Mellitus (TNDM)
643(1)
Permanent Neonatal Diabetes Mellitus (PNDM)
643(2)
Syndromic Neonatal Diabetes Mellitus
645(1)
Diagnosis
645(1)
Treatment
646(1)
Rare Forms of Diabetes
647(1)
Defects in Insulin Secretion
647(1)
Living with Diabetes
648(1)
Education
648(1)
Employment
648(1)
Driving
649(1)
References
649(22)
16 Disorders Associated with Hypoglycaemia in Children 671(30)
Pratik Shah
Emma Footit
Ritika Kapoor
Introduction
671(1)
Physiology of Blood Glucose Control
672(1)
Glucose Production
672(1)
Renal Contribution to Glucose Homeostasis
672(1)
Glucose Utilization
672(1)
Role of Gut Hormones in Glucose Homeostasis
673(1)
Metabolic Adaptation to Birth
673(1)
Metabolic Adaptation to Feeding and Fasting
674(1)
The Regulation of Insulin Secretion and Role of KATP Channels
675(1)
Glucose-Stimulated Insulin Secretion (GSIS)
675(1)
Definition of Hypoglycaemia
676(2)
Screening
677(1)
Numerical Cut-Offs Used in Clinical Practice
677(1)
Aetiology and Clinical Approach to Hypoglycaemia
678(2)
Age of Onset
678(1)
Past History
678(1)
Pregnancy, Birth and Neonatal History
679(1)
Family History
680(1)
Dietary and Drug History
680(1)
Examination
680(1)
Investigations for Hypoglycaemia
680(2)
Urgent Investigations
680(1)
Fast Provocation Test
680(1)
Other Planned Investigations
681(1)
Emergency Management of Hypoglycaemia
682(1)
Causes of Hypoglycaemia
682(11)
Hyperinsulinaemic Hypoglycaemia
682(5)
Hypoketotic Hy1oinsulinaemic Hypoglycaemia
687(1)
Factitious Hypoglycaemia
687(1)
Failure of Counter-Regulatory Hormones
688(1)
Inborn Errors of Metabolism Presenting with Hypoglycaemia
689(4)
References
693(8)
17 Obesity 701(28)
Wieland Kiess
Introduction
701(1)
Definitions, Differential Diagnosis, Assessments and Measurements
701(2)
Aetiology of Obesity
703(2)
Common or Multifactorial Obesity and Fetal Programming
705(1)
Neurobiology of Satiety and Hunger
705(1)
Hedonistic Signals and Addiction
706(1)
Behaviour, Hypothalamus and Obesogenic Environment
707(1)
Biology of Adipose Tissue and Adipocytes
707(1)
Microbiota
708(1)
Endocrinology of Obesity
709(1)
Epigenetics
709(1)
Social Inheritance
709(1)
Sociodemographics
710(1)
Nutrition and Malnutrition
710(1)
Physical Activity
711(1)
Sedentary Behaviour
711(1)
Endocrine-Disrupting Chemicals and Toxicology
711(1)
Media Use
712(1)
Cultural Aspects
712(1)
Evolution
712(1)
Epidemiology
713(1)
Developed Countries
713(1)
Developing Countries
713(1)
Co-Morbidities and Consequences
713(5)
Carbohydrate Metabolism
714(1)
Lipid Metabolism
715(1)
Cardiovascular
715(1)
Skeletal System
715(1)
Non-Alcoholic Fatty Liver Disease (NAFLD, NASH)
716(1)
Metabolic Syndrome
716(1)
Urogenital
717(1)
Puberty and Fertility
717(1)
Psychology and Psychiatric Co-Morbidity
718(1)
Social Participation
718(1)
Mortality
719(1)
Health Economics
720(3)
Treatments
720(1)
Medical Management
720(1)
Multidisciplinary Therapeutic Approach
720(1)
Nutrition Treatment and Dieting
721(1)
Physical Activity Training
721(1)
Behavioural Therapies
721(1)
Family-Based Therapies and Community-Based Therapies
721(1)
Bariatric Surgery
721(1)
Pharmacotherapy
722(1)
Prevention
722(1)
Community and Society
723(1)
Microbiota
723(1)
Urban Living
724(1)
Advertising Industries
724(1)
Conclusions
725(1)
Further Reading
726(2)
Weblinks
728(1)
18 Genetic Obesity Syndromes 729(8)
Tinh-Hai Collet
I. Sadaf Farooqi
Introduction
729(1)
Genetic Contributors to Obesity: The Evidence
729(1)
Genetic Obesity Syndromes: An Overview
730(1)
Obesity with Developmental Delay
730(2)
Prader-Willi Syndrome
730(1)
Albright's Hereditary Osteodystrophy
731(1)
Bardet-Biedl Syndrome
731(1)
BDNF and TrkB Deficiency
731(1)
SIM1 Deficiency
731(1)
Obesity Without Development Delay
732(2)
Leptin and Leptin Receptor Deficiency
732(1)
Disorders Affecting Pro-Opiomelanocortin (POMC) and POMC Processing
733(1)
PC1/3 (PCSK1) Deficiency
733(1)
MC4R Deficiency
733(1)
SH2B1 Deficiency
734(1)
KSR2 deficiency
734(1)
Conclusions
734(1)
References
734(2)
Weblinks
736(1)
19 Endocrine Care During Adolescence into Young Adulthood 737(20)
Helena Gleeson
Introduction
737(1)
Adolescence and Young Adulthood
737(3)
Biopsychosocial Development and Growing Up with an Endocrine Condition
737(3)
Exploratory and Health-Related Behaviours
740(3)
Developmentally Appropriate Healthcare
740(1)
Designing Services to Meet Young People's Needs
740(1)
Training Healthcare Providers
741(1)
Clinic Consultations
741(2)
Addressing Adherence
743(1)
Involving Parents
743(1)
Transition and Transfer to Adult Services
744(1)
Evidence Base for Transition and Transfer
744(1)
Monitoring Transition and Transfer
744(1)
Young People with Endocrine Conditions
744(6)
Endocrine Care in Adolescence
746(1)
Symptoms and Signs of PCOS in Adolescence
746(4)
Conclusion
750(1)
References
751(6)
Index 757
MEHUL T. DATTANI, MD, FRCP, FRCPCH, is Professor of Pediatric Endocrinology at the UCL GOS Institute of Child Health and Head of Pediatric Endocrinology at Great Ormond Street Hospital for Children, University College London Hospitals, and Institute of Child Health. He is currently the Chair of the Programme Organising Committee of the European Society for Paediatric Endocrinology.

CHARLES G.D. BROOK, MA, MD, FRCP, was the first Professor of Pediatric Endocrinology in the UK and the founder of the London Centre for Pediatric Endocrinology at Great Ormond Street Hospital and University College London Hospitals. He was the recipient of the Andrea Prader Prize in 2000, the most prestigious award for outstanding leadership and research in the gift of the European Society for Paediatric Endocrinology.