Category:Paediatrics

A

• Category:Autoimmune encephalitis

C

• Category:Child development
• Category:Congenital diseases
• Category:Congenital heart disease

D

• Category:Dwarfism

E

• Category:Embryopathies

I

• Category:Inborn error of metabolism

K

• Category:Kallmann syndrome

L

• Category:Lysosomal storage diseases

M

• Category:Muscular dystrophies

N

• Category:Neonatology

P

• Category:Paediatric surgery
• Category:Periodic syndromes

S

• Category:Spinal muscular atrophies

A

• Achondroplasia
• Acute lymphoblastic leukaemia
• Alice in Wonderland syndrome
• Anisospondyly
• Aseptic meningitis
• Attention deficit hyperactivity disorder
• Atypical mycobacterial lymphadenitis
• Autism
• Autoimmune encephalitis
• Autoimmune epilepsy

B

• BCS1L
• Baby
• Bacterial meningitis
• Bamforth-Lazarus syndrome
• Bardet-Biedl syndrome
• Becker muscular dystrophy
• Biliary atresia
• Blalock-Taussig shunt
• British National Formulary for Children
• Bronchiolitis

C

• CINCA
• Cardiff cards
• Cardiofaciocutaneous syndrome
• Carney triad
• Carnitine palmitoyltransferase I deficiency
• Carnitine palmitoyltransferase II deficiency
• Carnitine-acylcarnitine translocase deficiency
• Central precocious puberty
• Cerebrospinal fluid
• Chickenpox
• Child
• Child protection
• Childhood vaccination schedule
• Cholinergic urticaria
• Chronic granulomatous disease
• Chronic idiopathic urticaria
• Chronic infantile neurological, cutaneous, articular syndrome
• Coarctation of the aorta
• Coenzyme Q deficiency
• Combined pituitary hormone deficiency 5
• Congenital adrenal hyperplasia
• Congenital deafness
• Congenital heart disease
• Cow's milk protein intolerance
• Craniopharyngioma
• Cri-du-chat syndrome
• Croup
• Culler-Jones syndrome
• Cystic fibrosis

D

• Deprivation of liberty safeguards
• Development of the heart
• Developmental dysplasia of the hip
• Diabetic ketoacidosis
• Distal hereditary motor neuronopathy
• Distal spinal muscular atrophy
• Down syndrome
• Dravet syndrome
• Drugs in lactation
• Duchenne muscular dystrophy
• Dyslexia
• Dyssynergia cerebellaris myoclonica

E

• EMLA

E cont.

• Epiglottitis
• Examination of the newborn

F

• Failure to thrive
• Familial amyotrophic lateral sclerosis
• Familial haemophagocytic lymphohistiocytosis
• Familial spastic paraparesis
• Febrile convulsion
• Fetal alcohol syndrome
• Focal cortical dysplasia of Taylor balloon cell type
• Foramen ovale
• Fragile X
• Friedreich's ataxia

G

• Glutathione synthetase deficiency
• Growth and development
• Growth hormone deficiency with pituitary anomalies
• Guthrie card

H

• Haemolytic disease of the newborn
• Haemophagocytic lymphohistiocytosis
• Haemophagocytic syndrome
• Harlequin change
• Hedgehog signalling pathway
• Hemihyperplasia
• Hermansky-Pudlak syndrome
• Hirschsprung disease
• Holoprosencephaly 9
• Hyper-IgE syndrome
• Hypertrichotic osteochondrodysplasia
• Hypogonadotropic hypogonadism-6

I

• Idiopathic scrotal oedema
• Immunodeficiency
• Immunodeficiency-centromeric instability-facial anomalies syndrome
• Infant
• Infant gastro-oesophageal reflux
• Infantile colic
• Infantile hypertrophic pyloric stenosis
• Infantile spasms
• Infantile striatonigral degeneration
• Insulin-like growth factor 1 resistance
• Intellectual disability
• Intraosseous access
• Irlen syndrome

J

• Johanson-Blizzard syndrome
• Joubert's syndrome
• Juvenile Paget's disease
• Juvenile idiopathic arthritis
• Juvenile onset recurrent respiratory papillomatosis

K

• Kallmann syndrome
• Kawasaki disease
• Kugelberg-Welander syndrome

L

• Lennox-Gastaut syndrome
• Loeys-Dietz syndrome

M

• Marino Ortolani
• Measles
• Meconium ileus
• Medium-chain acyl-coenzyme A dehydrogenase deficiency
• Menarche
• Meningitis
• Meningitis case definitions
• Meningitis charities
• Meningitis checklist
• Meningitis prevention
• Meningococcal disease

M cont.

• Meningococcal meningitis
• Mitochondrial diseases
• Mosaic variegated aneuploidy syndrome
• Munchausen's syndrome by proxy
• Myopathic carnitine deficiency
• Myotonic dystrophy

N

• NOMID
• National Society for the Prevention of Cruelty to Children
• Neonate
• Neonates
• Nephroblastoma
• Nephronophthisis
• Nodding syndrome
• Non-accidental injury
• Nonprogressive spinal muscular atrophy
• Noonan syndrome

O

• Ortolani test

P

• Paediatric inguinal hernia
• Paediatric pharmacology
• Paediatric venepuncture
• Palivizumab
• Pendred syndrome
• Periodic syndrome
• Pertussis
• Phenylketonuria
• Physical urticaria
• Precocious puberty
• Progeria
• Proximal spinal muscular atrophy
• Puberty
• Pulmonary alveolar proteinosis
• Pulmonary hypertension
• Purpura fulminans
• Pycnodysostosis

R

• Rasmussen's encephalitis
• Reflex anoxic seizure
• Reibergrams
• Retinoblastoma
• Retrolental hyperplasia
• Rett syndrome
• Reye's syndrome
• Rickets
• Royal College of Paediatrics and Child Health

S

• Senior-Loken syndrome
• Septic arthritis
• Septooptic dysplasia
• Soiling
• Spinal and bulbar muscular atrophy
• Spinal muscular atrophy
• Sub-acute sclerosing panencephalitis
• Sudden unexpected death in infancy
• Syndromic microphthalmia 5
• Systemic carnitine deficiency
• Systemic juvenile idiopathic arthritis

T

• TORCH syndrome
• Takayasu arteritis
• Teething
• Thalassaemia
• Thelarche
• Tinea capitis
• Torticollis
• Total parenteral nutrition