Great Ormond Street Handbook of Paediatrics Second Edition

Description:

 

The product of a world center of excellence in teaching and medical and surgical practice, second edition of a bestseller combines the advantages of a colour atlas with those of a short textbook covering clinical features, epidemiology, investigations, and differential diagnosis. Illustrations include clinical photos, imaging, charts, graphs, and histology where appropriate. The author/editor team, supported by specialist contributions from clinicians at Institute of Child Health/Great Ormond Street, offers an unmatched range of expertise in a compact volume. The book is of lasting reference value to pediatricians in training and practice, and to professionals in many other disciplines.

 

Table of Contents:

 

Chapter 1 Emergency Medicine

Introduction

Upper airway obstruction

Anaphylaxis

Asthma

Bronchiolitis

Cardiac emergencies

Cyanosis

Cardiogenic pulmonary oedema

Cardiogenic shock

Arrhythmias

Acute encephalopathic illness

Convulsive status epilepticus

Other encephalopathic illness

Diabetic ketoacidosis

Acute respiratory distress syndrome

Sepsis

Trauma

Traumatic brain injury

The child with multiple injuries

Burns

Poisoning

References/further reading

Chapter 2 Child Protection

Introduction

Types of abuse and neglect

Paediatric assessment of a child with suspicion of maltreatment

Physical abuse

Neglect

Sexual abuse

Other considerations in child protection

What to do when abuse is suspected

Further reading

Chapter 3 Infectious Diseases

Bacteria

Diphtheria

Tetanus

Meningococcal infections

Tuberculosis

Tuberculous meningitis

Non-tuberculous mycobacterial infections

Cat-scratch disease

Lyme disease

Pyogenic liver abscess

Staphylococcal toxic shock syndrome

Tularaemia

Viruses

HIV infection and AIDS

Congenital cytomegalovirus

Infectious mononucleosis

Measles

Neonatal herpes simplex virus

Varicella (chicken pox)

Herpes zoster (shingles)

Protozoa/fungi/tropical diseases/miscellaneous

Congenital toxoplasmosis

Cryptosporidiosis

Cysticercosis (neurocysticercosis)

Invasive aspergillosis

Neonatal systemic candidiasis

Malaria

Schistosomiasis (urinary)

Visceral leishmaniasis (Kala-azar)

Kawasaki disease

Further reading

Chapter 4 Respiratory Medicine

Cystic fibrosis

Chronic lung disease of prematurity

Preschool wheeze

Asthma

Bronchiolitis

Pneumonia

Empyema

Non-CF bronchiectasis

Interstitial lung disease

Chronic aspiration

Pneumothorax

Pierre Robin sequence

Pulmonary agenesis, aplasia and hypoplasia

Scimitar syndrome

Congenital pulmonary airway malformations

Lung transplantation

Further reading

Chapter 5 Cardiology

Developmental cardiology

Cardiac assessment

Congenital heart disease

Ventricular septal defect

Patent ductus arteriosus

Pulmonary stenosis

Coarctation of the aorta

Atrial septal defect

Fallot tetralogy

Aortic stenosis

Transposition of the great arteries

Hypoplastic left heart

Atrioventricular septal defect

Other cardiac lesions

Total anomalous pulmonary venous drainage

Tricuspid atresia

Double inlet left ventricle

Pulmonary atresia with an intact septum

Pulmonary atresia with a VSD

Ebstein anomaly

Interrupted aortic arch and truncus arteriosus

Congenitally corrected transposition

Vascular ring and sling

Heart muscle disease

Dilated cardiomyopathy

Myocarditis

Pericarditis

Hypertrophic cardiomyopathy

Restrictive cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy

Endocarditis

Kawasaki disease

Arrhythmias

Heart transplantation

Further reading

Chapter 6 Dermatology

Vascular lesions – tumours

Infantile haemangioma

Rare vascular tumours

Vascular lesions – malformations

Capillary malformations

Venous malformations

Arteriovenous malformations

Pigmentary lesions

Postinflammatory pigmentary changes

Vitiligo

Hypomelanotic macules

Pigmentary mosaicism

Café-au-lait macules

Congenital melanocytic naevi

Blistering conditions

Epidermolysis bullosa

Immunobullous disorders

Inflammatory conditions

Eczema

Morphoea (localised scleroderma)

Psoriasis

Lumps and bumps

Anogenital warts

Molluscum contagiosum

Sebaceous naevus

Aplasia cutis

Other important conditions

Acrodermatitis enteropathica

Incontinentia pigmenti

Cutaneous mast cell disease

Ichthyosis

Linear epidermal naevi

Ectodermal dysplasia

Paediatric dermatological emergencies

Stevens-Johnson syndrome and toxic epidermal necrolysis

Staphylococcal scalded skin syndrome

Collodion baby and harlequin ichthyosis

Eczema herpeticum

Generalised pustular psoriasis

Malignant skin conditions

Further reading

Chapter 7 Ophthalmology

Anatomy of the eye

Visual development

Lids

Ablepharon

Cryptophthalmos

Coloboma

Epicanthus

Entropion

Ectropion

Symblepharon

Blepharitis

Stye

Molluscum contagiosum

Capillary haemangioma

Port wine stain

Ptosis

Lid retraction

Preseptal cellulitis

Lid lag

The watering eye

Cornea – developmental disorders

Microcornea

Cornea plana

Megalocornea

Keratoconus

Congenital corneal opacification

Corneal dystrophies

Posterior embryotoxon

Corneal deposits

Keratitis

Conjunctiva

Infection-related conjunctivitis

Non infection-related conjunctivitis

Conjunctival pigmentation

Elevated conjunctival lesions

Diffusely elevated conjunctival lesions

Sclera

Pigmentation of the sclera

Scleral inflammation

Developmental anomalies of the globe

Nanophthalmos

Simple microphthalmos

Complex microphthalmos

Anophthalmia

Iris

Congenital iris defects

Acquired iris defects

Changes in iris colour

Leukaemia/lymphoma

Heterochromia irides

Pupil anomalies

Leukocoria

Dyscoria

Miosis

Mydriasis

Corectopia

Anisocoria

Lens anomalies

Aphakia

Abnormal shape

Dislocated lens

Lens opacity

Retinal anomalies

Haemorrhages

Hard exudates

Cotton wool spots

Retinal neovascularisation

Retinal vasculitis

Foveal hypoplasia

Maculopathy

Coloured macular lesions

Pale retinal lesions

Non-inflammatory lesions

Retinal detachment

Folds in the fundus

The optic disc

Optic disc swelling

Optic atrophy

Small optic disc

Large optic disc

Large optic disc cup

Optic disc vascular abnormalities

Optic disc haemorrhages

Lesions obscuring the optic disc

The orbit

Abnormalities of globe position

Lacrimal gland enlargement

Eye movement disorders

Ocular deviation in primary gaze

Anomalous eye movements

Abnormal head positions

Nystagmus

Further reading

Chapter 8 Neurology

Neurological examination: cranial nerves

The eye

Ptosis

Myasthenia

Disorders of eye movement

Third nerve palsy

Fourth nerve palsy

Sixth nerve palsy

Ophthalmoplegia

Upward gaze palsy

Lateral gaze palsy

Facial palsy

Lower motor neuron facial palsy

Upper motor neuron facial palsy

Lower cranial nerve abnormalities

Motor system

Pyramidal disorders

Extrapyramidal disorders

Wilson disease

Sydenham chorea and other poststreptococcal movement disorders

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis

Sandifer syndrome

Segawa syndrome (DOPA-responsive dystonia)

Ataxia

Ataxia telangiectasia

Friedreich ataxia

Acute generalised weakness in a previously well child

Guillain-Barré syndrome

Dermatomyositis

Spinal cord disorders

Hypotonia in infancy

Myotonic dystrophy (DM1)

Spinal muscular atrophy (SMA) type 1 (Werdnig-Hoffman disease)

Spinal muscular atrophy (SMA) type 2 and type 3

Chronic and progressive weakness in the older child

Duchenne/Becker muscular dystrophy

Hereditary motor and sensory neuropathy (CMT)

Cerebral palsy

Spina bifida

Headaches

Migraine

Psychogenic headaches

Intracranial hypertension

Idiopathic intracranial hypertension (‘benign’ intracranial hypertension, pseudotumour cerebri)

Macrocephaly

Hydrocephalus

Brain tumours

Learning difficulties

Epilepsy

Neurological and cognitive deterioration

Common conditions with neurological deterioration

Coma and acute encephalopathies

Stroke

Further reading

Chapter 9 Gastroenterology

Clinical presentation

Acute gastroenteritis

Faltering growth/failure to thrive

Constipation

Infantile colic

Recurrent abdominal pain

Toddler’s diarrhoea

Chronic intractable diarrhoea

Chronic intestinal failure

Gastrointestinal diagnoses

Fabricated and induced illness

Coeliac disease

Food allergic enteropathy

Autoimmune enteropathy

Eosinophilic gastrointestinal disease

Eosinophilic oesophagitis

Eosinophilic enteropathy

Eosinophilic disease of the colon (EDC) allergic colitis

Classic inflammatory bowel disease

Ulcerative colitis

Crohn disease

Lymphangiectasia

Ulcers

Gastric ulcer

Duodenal ulcers

Polyps

Isolated inflammatory/juvenile polyp

Juvenile polyposis syndrome

Familial polyposis coli and Gardner syndrome

Peutz-Jegher syndrome

Infections and infestations

Bacterial enteric infections

Feeding difficulties

Gastro-oesophageal reflux

Cyclical vomiting

Intestinal pseudo-obstruction

Short bowel syndrome

Congenital and inherited disorders

Congenital chloride diarrhoea

Glucose-galactose malabsorption

Sucrose-isomaltase deficiency

Lactose malabsorption

Pancreatic disease

Cystic fibrosis

Shwachman-Bodian-Diamond syndrome

Acute pancreatitis

Chronic pancreatitis

Liver disease

Primary sclerosing cholangitis

Chronic hepatitis

Acute hepatitis

Alagille syndrome

Mineral disorders (deficiencies, high level poisoning)

Zinc deficiency

Iron deficiency

Copper deficiency

Copper excess: Wilson disease

Selenium deficiency

Vitamin deficiencies

Scurvy, vitamin C/ascorbic acid deficiency

Beriberi, vitamin B1/thiamin deficiency

Pellagra, niacin deficiency

Riboflavin/vitamin B2 deficiency

Pyridoxine/vitamin B6 deficiency

Cyanocobalamin/vitamin B12 deficiency

Vitamin K/napthaquinone deficiency

Retinol/vitamin A deficiency

Tocopherol/vitamin E deficiency

Vitamin D deficiency

Further reading

Chapter 10 Renal Diseases

Acute kidney injury

Haemolytic uraemic syndrome

Glomerulonephritis

IgA vasculitis

Nephrotic syndrome

Chronic kidney disease

Cystic kidney diseases

Congenital anomalies of the kidney and urinary tract

Vesicoureteric reflux

Renovascular hypertension

Renal Fanconi syndrome

Further reading

Chapter 11 Haematology

Non-Hodgkin lymphoma

Haematological disorders and Down syndrome

Transient myeloproliferative disorder

Myeloid leukaemia and DS

Acute lymphoblastic leukaemia and DS

Acute promyelocytic leukaemia and thrombosis

Congenital (monocytic and myelomonocytic) leukaemia

Ophthalmic extramedullary leukaemic deposits

Granulocytic sarcoma

Hypopyon

Severe aplastic anaemia

Juvenile myelomonocytic leukaemia

Paediatric myelodysplastic syndromes

Fanconi anaemia

Dyskeratosis congenita and TINF2 mutations

Hypereosinophilic syndrome and T(5;12)

Acute febrile neutrophilic dermatosis – Sweet syndrome

Myelofibrosis and systemic lupus erythematosus

Infant megaloblastic anaemia: transcobalamin II deficiency

Congenital erythropoietic porphyria

Kasabach-Merritt syndrome

Thrombocytopenia absent radius

Bernard-Soulier syndrome

von Willebrand disease

Severe haemophilia A and B (classic haemophilia and Christmas disease)

Red cell membrane abnormalities

Hereditary elliptocytosis

Hereditary spherocytosis

Beta-thalassaemia major

Sickle cell disease

Glucose-6-phosphate dehydrogenase deficiency

Pyruvate kinase deficiency

Further reading

Chapter 12 Oncology

Introduction

Renal tumours

Liver tumours

Langerhans cell histiocytosis

Rhabdomyosarcoma, other soft tissue sarcomas and fibromatosis

Rhabdomyosarcoma

Other soft tissue sarcomas

Neuroblastoma

Very low- and low-risk neuroblastoma

Intermediate-risk neuroblastoma

High-risk neuroblastoma

Retinoblastoma

Ewing sarcoma and peripheral primitive neuroectodermal tumour

Osteosarcoma

Extracranial malignant germ cell tumours

Tumours of the central nervous system

Ependymoma

Medulloblastoma/PNET

High-grade supratentorial glioma

Brainstem glioma

Low-grade astrocytoma

Rare tumours

Thyroid carcinoma

Nasopharyngeal carcinoma

Adrenocortical carcinoma

Renal cell carcinoma

Late effects of cancer treatment

Further reading

Chapter 13 Endocrinology

The short child

Growth hormone deficiency/ insufficiency

Laron-type dwarfism

Low birth weight syndrome

Turner syndrome

Prader-Willi syndrome

Skeletal dysplasias

The tall child

Marfan syndrome

Pituitary gigantism

Late puberty

Klinefelter syndrome

Early puberty

Premature thelarche/thelarche variant or ‘benign’ precocious puberty

Gonadotrophin-dependent (central) precocious puberty

McCune-Albright syndrome

Polycystic ovarian disease

Thyroid disorders

Congenital hypothyroidism

Acquired hypothyroidism

Graves disease

Adrenal disorders

Primary adrenal insufficiency

Cushing syndrome

Ambiguous genitalia

Congenital adrenal hyperplasia

Disorders of glucose homeostasis

Hyperinsulinism

Type 1 diabetes mellitus

Type 2 diabetes mellitus

Monogenic diabetes

Insulin resistance syndromes

Other forms of diabetes

Disorders of calcium metabolism

Rickets

Hypoparathyroidism/pseudohypoparathyroidism

Hypercalcaemia

Williams syndrome

Further reading

Chapter 14 Metabolic Diseases

Adrenoleukodystrophy

Gaucher disease

Hurler disease, MPS I

Sanfilippo syndrome, MPS III

Morquio syndrome, MPS IV

Homocystinuria – classical and secondary to remethylation disorders

Wolman/cholesterol ester disease

Fructose 1,6-bisphosphatase deficiency

Neuronal ceroid lipofusinoses

Urea cycle disorders

Galactosaemia

Fatty acid oxidation defects

Disorders of ketone body metabolism

Tyrosinaemia

Glycogen storage disease type I

Peroxisomal biogenesis disorders

Leigh syndrome

Pyruvate dehydrogenase deficiency

Pyruvate carboxylase deficiency

Menke disease

Phenylketonuria

Biotin disorders

Glutaric acidaemia type I

GLUT 1 transporter deficiency

Fabry disease

Pompe disease

Creatine deficiency disorders

Methylmalonic and propionic acidaemia (MMA, PA)

Neurotransmitter disorders (L-dopamine-responsive dystonia, tyrosine hydroxylase deficiency, pterin disorders)

Sphingolipidosis disorders (Tay Sachs/Sandhoff/GM1/Niemann-Pick/metachromatic dystrophy/Krabbe)

Congenital disorders of glycosylation

Non-ketotic hyperglycinaemia (glycine encephalopathy)

Smith-Lemli-Opitz syndrome

Hypercholesterolaemia

Further reading

Chapter 15 Genetics

Introduction

Common congenital malformations

Chromosome disorders

Chromosomes – structural abnormalities and imbalance

Robertsonian translocation

Chromosome mosaicism

Trisomy 13 (Patau syndrome)

Trisomy 18 (Edwards syndrome)

Trisomy 21 (Down syndrome)

Turner syndrome, 45, X and variants

Williams syndrome

22q11 deletion syndrome (DiGeorge syndrome)

Single gene disorders

Autosomal dominant inheritance

Autosomal recessive inheritance

X-linked inheritance

Mitochondrial conditions and inheritance

Genetic syndromes with cardiac malformation as a major feature

The floppy baby

Prader-Willi syndrome

Myotonic dystrophy (myotonic dystrophy typ)

Syndromes associated with features of a connective tissue disorder

Children with severe developmental delay

Angelman syndrome

Rett syndrome

Other common single gene disorders

Duchenne muscular dystrophy

Fragile X syndrome

Neurofibromatosis type 1

Tuberous sclerosis

Other rare recognisable syndromes

Kabuki syndrome

Rubinstein-Taybi syndrome

de Lange syndrome

Sotos syndrome

Goldenhar syndrome (hemifacial microsomia)

VATER/VACTERL association

Bardet-Biedl syndrome

Beckwith-Wiedemann syndrome

Silver-Russell syndrome

Albright hereditary osteodystrophy (pseudohypoparathyroidism type 1a)

Further reading

Chapter 16 Immunology (Primary Immunodeficiency Syndromes)

Background

I Combined immunodeficiencies

Severe combined immunodeficiency

Specific SCID sub-types

Omenn syndrome (SCID variant)

Adenosine deaminase (ADA) deficiency

II Other well-defined syndromes

Wiskott-Aldrich syndrome

Cartilage hair hypoplasia

Ataxia telangiectasia

III Thymic defects

DiGeorge syndrome

IV Antibody deficiency syndromes

Common variable immunodeficiency

X-linked agammaglobulinaemia (Bruton disease)

Hypogammaglobulinaemia with hyper-IgM (class-switch recombination [CSR] defects) (including CD40 ligand deficiency)

V Hyper-IgE syndromes

Autosomal dominant hyper-IgE syndrome

Autosomal recessive hyper-IgE syndrome

VI Defects of immune regulation

X-linked lymphoproliferative disease (Duncan syndrome)

Chediak-Higashi syndrome

Autoimmune lymphoproliferative syndrome

Chronic mucocutaneous candidiasis

VII Phagocytic defects

Chronic granulomatous disease

Leukocyte adhesion deficiencies

VIII Innate immune defects

X-linked immunodeficiency associated with ectodermal dysplasia

Interferon-gamma/IL-12 pathway defects

Further reading

Chapter 17 Rheumatology

Introduction

Juvenile idiopathic arthritis

Systemic JIA

Polyarticular onset: rheumatoid factor (RF)-negative JIA

Polyarticular onset: RF-positive JIA

Oligoarticular arthritis

Enthesitis-related arthritis

Psoriatic arthritis

Arthritis associated with other chronic diseases

Scleroderma

Systemic sclerosis

Localised scleroderma (morphoea)

Juvenile dermatomyositis

Vasculitides

Henoch Schönlein purpura (IgA vasculitis)

Kawasaki disease

Polyarteritis nodosa

Anti-neutrophil cytoplasmic antibody-associated vasculitides

Takayasu arteritis

Systemic lupus erythematosus

Overlap connective tissue disease

Chronic recurrent multifocal osteomyelitis

Periodic fever syndromes/autoinflammatory diseases

Introduction

Familial Mediterranean fever

Tumour necrosis factor receptor-associated periodic syndrome

Mevalonate kinase deficiency/hyperimmunoglobulin D periodic fever syndrome

Cryopyrin-associated periodic syndrome

Periodic fever, aphthous stomatitis, pharyngitis and adenitis

Chronic pain syndrome

Complex regional pain syndrome

Joint hypermobility syndrome

Further reading

Chapter 18 Neonatal and General Paediatric Surgery

Oesophageal atresia

Congenital diaphragmatic hernia

Neonatal intestinal obstruction

Meconium ileus

Duodenal atresia

Intestinal atresia

Anorectal anomalies

Hirschsprung disease

Malrotation

Duplications of the alimentary tract

Necrotising enterocolitis

Exomphalos

Gastroschisis

Umbilical hernia

Umbilical anomalies

Gastrointestinal haemorrhage

Meckel diverticulum

Pyloric stenosis

Intussusception

Sacrococcygeal teratoma

Appendicitis

Neck lesions

Cystic hygroma

Branchial sinus/cyst

Preauricular sinus

Sacral sinuses

Dermoid cysts

Thyroglossal cysts/fistulae

Inguinal hernia

Hydrocoele

Undescended testis

Torsion of the testis

Phimosis

Biliary atresia

Choledochal cyst

Vascular malformations

Haemangioma

Congenital vascular malformations

Klippel-Trenaunay syndrome

Lymphoedema

Spina bifida

Conjoined twins

Further reading

Chapter 19 Otorhinolaryngology

Otitis media with effusion (‘glue ear’)

Acute otitis media

Cholesteatoma

Chronic suppurative otitis media

Otitis externa

Aural foreign bodies

Congenital anomalies of the ear

Preauricular sinus and abscess

External ear anomalies

Middle ear anomalies

Inner ear anomalies

Nasal polyps

Rhinosinusitis

Nasal glioma and meningoencephalocoele

Juvenile nasopharyngeal angiofibroma

Nasal foreign bodies

Choanal atresia

Tonsillitis (acute, chronic and recurrent)

Peritonsillar abscess (quinsy)

Retropharyngeal abscess

Obstructive sleep apnoea

Drooling

Laryngomalacia

Recurrent respiratory papillomatosis

Subglottic stenosis

Laryngeal and tracheobronchial foreign bodies

Branchial sinuses, fistulae and cysts

Paediatric head and neck masses

Thyroglossal duct cyst

Oropharyngeal and oesophageal foreign bodies

Further reading

Chapter 20 Plastic Surgery

Cleft lip and alveolus +/- palate

Cleft palate (isolated)

Congenital melanocytic naevi

Craniosynostosis

Epidermolysis bullosa

Extravasation

Hemifacial microsomia

Microtia and ear reconstruction

Proteus syndrome

Radial longitudinal deficiency

Vascular anomalies

Capillary malformations in later childhood

Infantile haemangioma

Acknowledgements

References

Chapter 21 Orthopaedics and Fractures Fractures

Normal variations of gait and posture

Congenital and developmental abnormalities of the lower limb

Postural abnormalities (the moulded baby)

Congenital talipes equinovarus deformity (‘the club foot’)

Congenital vertical talus

Developmental dysplasia of the hip

Leg length discrepancies

Fibula hemimelia

Proximal femoral focal deficiency

Congenital tibial deficiency

Common congenital toe problems

Other congenital/acquired lower limb problems

Blount disease

Congenital pseudarthrosis of the tibia

Posteromedial tibial bow

Pes cavus (the high arched foot)

Classic causes of lower limb pain

The child with a (painful) limp

Bone and joint infection (osteomyelitis and septic arthritis)

Transient synovitis vs. septic arthritis

Legg-Calvé-Perthes disease (often called Perthes disease)

Slipped upper femoral epiphysis

Upper limb abnormalities

Neonatal brachial plexopathy

Torticollis

Congenital upper limb anomalies

Radial club hand

Ulnar club hand

Radioulnar synostosis

Congenital dislocation of the radial head

Other minor upper limb abnormalities

Examples of generalised conditions affecting the musculoskeletal system

Benign joint hypermobility syndrome

Arthrogryposis

Neuromuscular conditions with orthopaedic concerns

Cerebral palsy

Spina bifida

The spine

Congenital deformities

Scoliosis

Scheuermann disease (kyphosis)

Spondylolisthesis

Back pain

Trauma

Specific paediatric injuries

Physeal injuries

Pulled elbow

Fractures around the elbow

Lower limb injuries

Pathological fractures

Further reading

Chapter 22 Urology

Congenital urine flow anomalies

Hydronephrosis/Dilatation

Pelviureteric junction anomaly (PUJA)

Vesicoureteric junction anomaly (megaureter)

Vesicoureteric reflux

Posterior urethral valve

Multi-cystic dysplastic kidney

Renal agenesis, ectopia and fusion

Duplex kidneys

Incontinence

Exstrophy-epispadias complex

Neuropathic bladder

Disorders of sex development

Hypospadias

Undescended testis

Acute scrotum

Urolithiasis

Neoplasia

Childhood renal tumours

Wilms tumour (nephroblastoma)

Genitourinary rhabdomyosarcoma

Further reading

Chapter 23 Allergic Diseases

Introduction: clarification of terms

General diagnostic approaches for allergies and adverse reactions to foods

Food allergy

Food-induced anaphylaxis

Asthma and allergic rhinitis: aspects related to food allergy

Allergic asthma

Atopic eczema

Chronic urticaria

Allergies/hypersensitivity to food additives

Drug hypersensitivity and adverse reactions to drugs

Management principles of cow’s milk and other food allergies

Further reading

Index

 

An aparitie	2016
Autor	Stephan Strobel, Lewis Spitz, Stephen D. Marks
Dimensiuni	3.2 x 17.8 x 24.8 cm
Editura	CRC Press
Format	Paperback
ISBN	9781482222791
Limba	Engleza
Nr pag	736