Children's Health

Allergic disease: The basics
Children's health 23 Dec 2005

Allergic disease: The basics

Allergic diseases include asthma, hay fever, eczema and hypersensitivity reactions. They occur when the immune system reacts against harmless substances.
Neuropathic pain (nerve pain)
Children's health 22 Dec 2005

Neuropathic pain (nerve pain)

Neuropathic pain does not help protect from injury like physiological pain, but is instead caused by an injury to or dysfunction of the nervous system.
Skin (epidermis) anatomy
Anatomy 22 Dec 2005

Skin (epidermis) anatomy

The skin or epidermis is the largest organ in the body. Layers of epidermis (skin) regulate temperature and sensation and create a protective barrier.
Muscular dystrophy
Bone 20 Dec 2005

Muscular dystrophy

Muscular dystrophies are a group of hereditary muscle diseases which cause progressive skeletal muscle weakness and symptoms like difficult walking.
Spina bifida
Bone 19 Dec 2005

Spina bifida

Spina bifida is a birth defect which is usually obvious in affected newborns. It occurs due to abnormal development of the neural tube in pregnancy.
Food allergy
Children's health 15 Dec 2005

Food allergy

Food allergies are common in children and adults. Peanuts, milk and dairy products, eggs, meat and fish are the most common food allergens.
LDL (Low Density Lipoprotein) Cholesterol Lowering
Blood 14 Dec 2005

LDL (Low Density Lipoprotein) Cholesterol Lowering

Low density lipoprotein cholesterol lowering therapies are used to treat high cholesterol levels and reduce the progression of heart disease.
Epileptic seizures (epileptic fits; status epilepticus)
Children's health 27 Oct 2005

Epileptic seizures (epileptic fits; status epilepticus)

Epileptic seizures cause a jerking and shaking movement and loss of consciousness which usually stops spontaneously. They affect blood flow to the brain.
Lennox-Gastaut syndrome (LGS; childhood epilepsy)
Children's health 26 Oct 2005

Lennox-Gastaut syndrome (LGS; childhood epilepsy)

Lennox-Gastaut syndrome is a rare type of childhood epilepsy which impairs child development but usually resolves by 8 years of age.