Childhood apraxia of speech is a type of speech disorder. It is present from birth. A child with this condition has problems making sounds correctly and consistently. Apraxia is a problem with the motor coordination of speech.
Aplastic anemia is a rare blood disorder that most often occurs in children, teens, and young adults. This piece offers helpful information on how to help your child live with this disease.
EDMD is a rare inherited muscle disease. It causes weakness in your child’s shoulders, upper arms, and calves. The disease also causes stiff joints that can’t move well.
Duchenne muscular dystrophy is a rare genetic condition that weakens your child's muscles. It appears in young boys, usually between ages 2 and 5.
Selective mutism is a rare condition in which a child can’t speak in certain settings but can speak fine in others. It can cause problems with school and social situations.
X-rays are a kind of imaging test that provides your healthcare provider with information about structures inside the body. These tests expose children to low doses of radiation.
Tongue-tie (ankyloglossia) is a problem with the tongue that is present from birth. It causes speech and eating problems in some children.
Open neural tube defects (ONTDs) are problems with the way the brain, spinal cord, or spine forms while a baby is growing in the mother's uterus.
Hemoglobin C disease is caused by abnormal hemoglobin, which is the part of red blood cells that carries oxygen to cells, tissues, and organs. Learn more about the condition, including causes, symptoms, and treatment.
A varicocele is when veins in the scrotum have become large and swollen (dilated). The condition is like varicose veins that occur in the legs. Here's what you need to know.