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Table Of Contents

CONTRIBUTORS
FOREWORD
PREFACE
INTRODUCTION
ANAPHYLAXIS
UPPER AIRWAY OBSTRUCTION
ASTHMA
BRONCHIOLITIS
CARDIAC EMERGENCIES
CYANOSIS
CARDIOGENIC SHOCK
SEPTIC SHOCK AND MULTI-ORGAN FAILURE
THE HEAD-INJURED CHILD
THE CHILD WITH MULTIPLE INJURIES
BURNS
DIABETIC KETOACIDOSIS
STATUS EPILEPTICUS
POISONING
SEDATION IN PICU
FORMS OF CHILD ABUSE
PHYSICAL ABUSE
BITE MARKS
BRUISES
BURNS AND SCALDS
FRACTURES
SHAKEN BABY SYNDROME
FABRICATED OR INDUCED ILLNESS
NEGLECT
SEXUAL ABUSE
MANAGEMENT OF CHILD ABUSE
BACTERIA
DIPHTHERIA
TETANUS
MENINGOCOCCAL INFECTIONS
TUBERCULOSIS
NON-TUBERCULOUS MYCOBACTERIAL INFECTIONS (NTM) Incidence
PYOGENIC LIVER ABSCESS
VIRUSES
HIV INFECTION AND AIDS
INFECTIOUS MONONUCLEOSIS
MEASLES
CRYPTOSPORIDIOSIS
INVASIVE ASPERGILLOSIS
MALARIA
KAWASAKI DISEASE
CYSTIC FIBROSIS
PNEUMONIA
CHRONIC ASPIRATION
PNEUMOTHORAX
EMPYEMA
PIERRE ROBIN ANOMALAD
TRACHEOBRONCHOMALACIA
DIAPHRAGMATIC HERNIA
FOREIGN BODY
PRIMARY CILIARY DYSKINESIA
MYCOPLASMA PNEUMONIAE
4.24Asphyxiating thoracic dystrophy
BRONCHOGENIC CYST
SCIMITAR SYNDROME
COARCTATION OF THE AORTA
(PAD)
TETRALOGY OF FALLOT (TOF)
PULMONARY STENOSIS
AORTIC STENOSIS
CARDIOMYOPATHY
SUPRAVENTRICULAR TACHYCARDIA (SVT)
HEART BLOCK
ENDOCARDITIS
TRICUSPID ATRESIA
VASCULAR RING
VIRAL WARTS
MOLLUSCUM CONTAGIOSUM
(ATOPIC ECZEMA)
SCABIES
HAEMANGIOMA
OROFACIAL HERPES SIMPLEX
PYOGENIC GRANULOMA
KELOID
PITYRIASIS VERSICOLOR
PITYRIASIS ROSACEA
VITILIGO
PSORIASIS
PORT WINE STAIN
URTICARIA PIGMENTOSA
ECZEMA HERPETICUM
ERYTHEMA MULTIFORME
ANOGENITAL WARTS
LICHEN STRIATUS
SEBACEOUS NAEVUS
VERRUCOUS EPIDERMAL NAEVI
INFANTILE ACNE VULGARIS
TUBEROUS SCLEROSIS
JUVENILE DERMATOMYOSITIS
INCONTINENTIA PIGMENTI
EPIDERMOLYSIS BULLOSA
ANATOMY OF THE EYE
VISUAL DEVELOPMENT
LIDS
COLOBOMA
SYMBLEPHARON
BLEPHARITIS
CAPILLARY HAEMANGIOMA
PTOSIS
LID RETRACTION
PRESEPTAL CELLULITIS
MYDRIASIS
CORECTOPIA
ANISOCORIA
LENS ANOMALIES
APHAKIA
ABNORMAL SHAPE
DISLOCATED LENS
LENS OPACITY
RETINAL ANOMALIES
HAEMORRHAGES
HARD EXUDATES
COTTON WOOL SPOTS
RETINAL NEOVASCULARIZATION
RETINAL VASCULITIS
MACULOPATHY
PALE RETINAL LESIONS
RETINAL DETACHMENT
FOLDS IN THE FUNDUS
THE OPTIC DISC
OPTIC ATROPHY
SMALL OPTIC DISC
LARGE OPTIC DISC
LARGE OPTIC DISC CUP
THE ORBIT
EYE MOVEMENT DISORDERS
OCULAR DEVIATION IN PRIMARY GAZE
MYASTHENIA
DISORDERS OF EYE MOVEMENT
FACIAL PALSY
LOWER CRANIAL NERVE ABNORMALITIES
WILSON’S DISEASE
SYDENHAM’S CHOREA
MOTOR SYSTEM
ATAXIA
FRIEDREICH’S ATAXIA
HYPOTONIA IN INFANCY
ACUTE GENERALIZED WEAKNESS IN A PREVIOUSLY WELL CHILD
DERMATOMYOSITIS
SPINAL CORD DISORDERS
CEREBRAL PALSY
SPINA BIFIDA
HEADACHES
MIGRAINE
PSYCHOGENIC HEADACHES
INTRACRANIAL HYPERTENSION
HYDROCEPHALUS
BRAIN TUMOURS
MACROCEPHALY
LEARNING DIFFICULTIES
EPILEPSY
KRABBE’S (GLOBOID CELL) LEUKODYSTROPHY
METACHROMATIC LEUKODYSTROPHY
TAY SACH’S DISEASE
LEIGH’S DISEASE
STROKE
ACUTE GASTROENTERITIS
FAILURE TO THRIVE
CONSTIPATION
INFANTILE COLIC
RECURRENT ABDOMINAL PAIN
TODDLER’S DIARRHOEA
CHRONIC INTRACTABLE DIARRHOEA
CHRONIC INTESTINAL FAILURE
FABRICATED AND INDUCED ILLNESS
COELIAC DISEASE
FOOD-SENSITIVE ENTEROPATHY
AUTOIMMUNE ENTEROPATHY
EOSINOPHILIC GASTROENTEROPATHY
CLASSIC INFLAMMATORY BOWEL DISEASE
ULCERATIVE COLITIS
CROHN’S DISEASE
ALLERGIC COLITIS
LYMPHANGIECTASIA
HELICOBACTER PYLORI
CAMPYLOBACTER JEJUNI
CLOSTRIDIUM DIFFICILE
SALMONELLA
PATHOGENIC ESCHERICHIA COLI
GIARDIA LAMBLIA
YERSINIA ENTEROCOLITICA
CRYPTOSPORIDIUM
CONGENITAL CHLORIDE DIARRHOEA
SUCROSE–ISOMALTASE DEFICIENCY
LACTOSE MALABSORPTION
ACUTE PANCREATITIS
LIVER DISEASE
SCLEROSING CHOLANGITIS
CHRONIC HEPATITIS
ACUTE HEPATITIS
ALAGILLE SYNDROME
MINERAL DEFICIENCIES
ZINC DEFICIENCY
IRON DEFICIENCY
COPPER DEFICIENCY
COPPER EXCESS: WILSON’S DISEASE
SELENIUM DEFICIENCY
VITAMIN DEFICIENCIES
SCURVY, VITAMIN C / ASCORBIC ACID DEFICIENCY
PELLAGRA / NIACIN DEFICIENCY
RETINOL / VITAMIN A DEFICIENCY
TOCOPHEROL / VITAMIN E DEFICIENCY
VITAMIN D DEFICIENCY
NEPHROTIC SYNDROME
POLYCYSTIC KIDNEY DISEASES
VESICO-URETERIC REFLUX AND ITS NEPHROPATHY
RENAL AGENESIS AND DYSPLASIA
CHILDHOOD HYPERTENSION DUE TO RENO-VASCULAR DISEASE
ACUTE RENAL FAILURE
HODGKIN’S LYMPHOMA
EXTRAMEDULLARY ACUTE LYMPHOBLASTIC LEUKAEMIA
THROMBOCYTOPENIA WITH ABSENT RADIUS (TAR)
FANCONI ANAEMIA
11.31Transcobalamin II deficiency
DYSKERATOSIS CONGENITA
BETA THALASSAEMIA MAJOR
PYRUVATE KINASE DEFICIENCY
SICKLE CELL DISEASE
HEREDITARY ELLIPTOCYTOSIS
IRON DEFICIENCY ANAEMIA
SIDEROBLASTIC ANAEMIA
LEISHMANIASIS
GAUCHER DISEASE
OSTEOPETROSIS
LIVER TUMOURS
LANGERHANS CELL HISTIOCYTOSIS
HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH)
NEUROBLASTOMA
RETINOBLASTOMA
OSTEOSARCOMA
EXTRACRANIAL MALIGNANT GERM CELL TUMOURS
EPENDYMOMA
HIGH-GRADE SUPRATENTORIAL GLIOMA
BRAIN STEM GLIOMA
LOW-GRADE ASTROCYTOMA
CARCINOMAS
THYROID CARCINOMA
SALIVARY GLAND TUMOURS
SKIN CANCERS
AMBIGUOUS GENITALIA
THE SHORT CHILD
TURNER SYNDROME
LOW BIRTH WEIGHT SYNDROME
SKELETAL DYSPLASIAS
LARON-TYPE DWARFISM
TALL STATURE
Tall stature
MARFAN SYNDROME
PITUITARY GIGANTISM
EARLY PUBERTY
POLYCYSTIC OVARIAN DISEASE
LATE PUBERTY
KLINEFELTER SYNDROME
CONGENITAL HYPOTHYROIDISM
ACQUIRED HYPOTHYROIDISM
CUSHING SYNDROME
RICKETS
GRAVES’ DISEASE
WILLIAMS SYNDROME
HYPERINSULINISM
DIABETES MELLITUS
TYPE 1 DIABETES
TYPE 2 DIABETES
ADRENOLEUKODYSTROPHY
HURLER’S DISEASE
UREA CYCLE DISORDERS
GALACTOSAEMIA
FATTY ACID OXIDATION DEFECTS
TYROSINAEMIA
LEIGH SYNDROME
MENKE’S DISEASE
PHENYLKETONURIA
BIOTIN DISORDERS
(TRISOMY 21)
(TRISOMY 18)
(TRISOMY 13)
(5P–)
TURNER SYNDROME (XO)
NOONAN SYNDROME
CHROMOSOME MOSAICISM
FRAGILE X SYNDROME
15.16Rubinstein-Taybi syndrome
15.17Rubinstein-Taybi syndrome
DE LANGE SYNDROME
ANGELMAN SYNDROME
FRONTONASAL DYSPLASIA
VATER ASSOCIATION
GOLDENHAR SYNDROME
CHARGE ASSOCIATION
VELOCARDIOFACIAL SYNDROME
MOEBIUS SYNDROME
STICKLER SYNDROME
Moebius syndrome
RUSSELL–SILVER SYNDROME
ACHONDROPLASIA
Achondroplasia
HYPOCHONDROPLASIA
OSTEOGENESIS IMPERFECTA
SOTOS SYNDROME
ROBINOW SYNDROME
EEC SYNDROME
COCKAYNE SYNDROME
APERT SYNDROME
Cockayne syndrome
PFEIFFER SYNDROME
Pfeiffer syndrome
CROUZON SYNDROME
HOLOPROSENCEPHALY
BLEPHAROPHIMOSIS, PTOSIS EPICANTHUS INVERSUS SYNDROME (BPES)
GREIG SYNDROME
ROBERTS SYNDROME
(BRUTON’S DISEASE)
CHRONIC MUCOCUTANEOUS CANDIDIASIS (CMC)
ATAXIA-TELANGIECTASIA
LEUKOCYTE ADHESION DEFECTS
DI GEORGE SYNDROME
HYPER IgE SYNDROME
SYSTEMIC ONSET JIA
POLYARTICULAR ONSET: RHEUMATOID FACTOR NEGATIVE JIA
POLYARTICULAR ONSET: RHEUMATOID FACTOR POSITIVE JIA
OLIGOARTICULAR ARTHRITIS
ENTHESITIS-RELATED ARTHRITIS
PSORIATIC ARTHRITIS
SCLERODERMA
SYSTEMIC SCLEROSIS
LOCALIZED SCLERODERMA
VASCULITIDES
OVERLAP CONNECTIVE TISSUE DISEASE (CTD)
PERIODIC FEVER SYNDROMES
FAMILIAL MEDITERRANEAN FEVER
OTHER GENETIC PERIODIC FEVERS
CHRONIC PAIN SYNDROME
FIBROMYALGIA
(ALGODYSTROPHY)
ALTERNATIVE AND AUGMENTATIVE COMMUNICATION (AAC)
ACQUIRED CHILDHOOD APHASIA
ACQUIRED CHILDHOOD DYSARTHRIA
ACQUIRED CHILDHOOD ARTICULATORY DYSPRAXIA
VOICE DISORDERS / DYSPHONIA
TRACHEOSTOMY
DYSPHAGIA
CRANIOFACIAL CONDITIONS
OESOPHAGEAL ATRESIA
MECONIUM ILEUS
DUODENAL ATRESIA
INTESTINAL ATRESIA
ANORECTAL ANOMALIES
SACROCOCCYGEAL TERATOMA
APPENDICITIS
NECK LESIONS
CYSTIC HYGROMA
PREAURICULAR SINUS
DERMOID CYSTS
THYROGLOSSAL CYSTS / FISTULAE
INGUINAL HERNIA
(OME, ‘GLUE EAR’)
ACUTE OTITIS MEDIA (AOM)
CHOLESTEATOMA
CHRONIC SUPPURATIVE OTITIS MEDIA (CSOM)
OTITIS EXTERNA
AURAL POLYPS
AURAL FOREIGN BODIES
PRE-AURICULAR SINUS AND ABSCESS
EXTERNAL EAR
MIDDLE EAR ANOMALIES
INNER EAR ANOMALIES
NASAL POLYPS
RHINOSINUSITIS
NASAL MASS
NASAL GLIOMA
POSTNASAL ANGIOFIBROMA
Nasal mass
NASAL FOREIGN BODIES
CHOANAL ATRESIA
TONSILLITIS (ACUTE, CHRONIC AND RECURRENT)
(QUINSY)
RETROPHARYNGEAL ABSCESS
LARYNGOMALACIA
SUBGLOTTIC STENOSIS
BRANCHIAL SINUSES AND CYSTS
THYROGLOSSAL DUCT CYST
DENTAL FLUOROSIS
GINGIVAL INFLAMMATION
21.4Herpetic gingivostomatitis
HERPETIC GINGIVOSTOMATITIS
TETRACYCLINE STAINING
FISSURE SEALANT
21.10Unerupted (displaced) upper left central incisor
21.8Retained deciduous incisor
RETAINED DECIDUOUS INCISORS
UNERUPTED (DISPLACED) UPPER LEFT CENTRAL INCISOR
DENTIGEROUS CYST
ODONTODYSPLASIA
AUTOTRANSPLANTATION
COMPLEX PERIODONTITIS
ENAMEL HYPOPLASIA
DENTINOGENESIS IMPERFECTA
(HYPOPLASTIC VARIETY)
INFECTED TOOTH GERM
FACIAL ABSCESS
DENS INVAGINATUS
HYPODONTIA
21.30Cervico-facial lymphadenitis
EOSINOPHILIC GRANULOMA
Eosinophilic granuloma
CONGENITAL EPULIS
21.36Benign migratory glossitis (geographic tongue)
(GEOGRAPHIC TONGUE)
MUCOUS CYST
TORSIONAL DEFORMITY
FLAT FEET
PES CAVUS
GENU VALGUM AND GENU VARUM
22.23Developmental dysplasiaof the hip
LIMB LENGTH DISCREPANCY
22.28Proximal femoral focal deficiency
PROXIMAL FEMORAL FOCAL DEFICIENCY
22.31Congenital tibial deficiency
22.30Congenital tibial deficiency
CONGENITAL TIBIAL DEFICIENCY
22.34Congenital fibular deficiency
CONGENITAL FIBULAR DEFICIENCY
SYNDACTYLY
POLYDACTYLY
22.46Congenital dislocation of radial head
PSEUDARTHROSIS OF THE CLAVICLE
SPRENGEL’S CONGENITAL SCAPULAR ELEVATION
CONGENITAL DISLOCATION OF RADIAL HEAD
22.47Radioulnar synostosis
RADIOULNAR SYNOSTOSIS
MADELUNG’S DEFORMITY
RADIAL CLUB HAND
ULNAR DEFICIENCY
SCOLIOSIS
BRACHIAL PLEXUS INJURIES
GROWTH PLATE INJURIES
22.65Supracondylar fracture of humerus
‘SPECIAL’ PAEDIATRIC FRACTURES
SUPRACONDYLAR FRACTURE OF THE HUMERUS
(EPI)CONDYLAR FRACTURE OF HUMERUS
RADIAL NECK FRACTURE
FOREARM FRACTURES
FEMORAL FRACTURES
PATELLAR FRACTURES
PROXIMAL TIBIAL FRACTURES
TRACTION INJURIES AND STRESS FRACTURES
NON-ACCIDENTAL FRACTURES
PATHOLOGICAL FRACTURES
TESTICULAR TUMOURS
HYPOSPADIAS
WILMS’ TUMOUR
PRUNE-BELLY SYNDROME
UROLITHIASIS
POSTERIOR URETHRAL VALVES
CRYPTORCHIDISM
23.30Ambiguous genitalia
ANOMALIES OF KIDNEY POSITION AND NUMBER
URETERAL DUPLICATION
VESICOURETERIC REFLUX
URETEROCOELE
HEART TRANSPLANTATION: ENDOMYOCARDIAL BIOPSY
LUNG FUNCTION MONITORING
TRANSBRONCHIAL BIOPSY
ACUTE ALLOGRAFT REJECTION
BRONCHIOLITIS OBLITERANS SYNDROME (BOS)
Index
P. 1
Paediatrics and Child Health

Paediatrics and Child Health

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Published by CRC Press
The product of a world centre of excellence in teaching and medical and surgical practice, this colour handbook 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, offer an unmatched range of expertise in a compact volume, of lasting reference value to paediatricians in training and practice, and to professionals in many other disciplines.
The product of a world centre of excellence in teaching and medical and surgical practice, this colour handbook 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, offer an unmatched range of expertise in a compact volume, of lasting reference value to paediatricians in training and practice, and to professionals in many other disciplines.

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Published by: CRC Press on Aug 26, 2010
Copyright:Traditional Copyright: All rights reservedISBN:9781840765625
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