Medications
Learning Center
DiGeorge syndrome (22q11.2 deletion syndrome)
This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other health problems.
Hydronephrosis
Learn about this condition that occurs when urine doesn't drain properly from the upper urinary tract, leading to kidney swelling.
Atypical genitalia
In this rare condition, a baby's genitals are not clearly male or female. Genitals may not be fully developed or the baby may have features of more than one sex.
Broken collarbone
This common injury is usually the result of falling, playing sports or being in a traffic accident.
Tay-Sachs disease
This rare, inherited disease causes a buildup of fatty acids that damages the brain and typically results in muscle control loss, blindness and paralysis.
Pulmonary atresia with intact ventricular septum
Also called PA/IVS, this rare congenital heart defect is diagnosed at or shortly after birth. Learn the symptoms and how it's treated.
Iron deficiency in children: Prevention tips for parents
Learn how much of this key mineral your child needs and what the health risks of not getting enough are.
Video: Ovulation
Ovulation — the release of an egg from an ovary — occurs about midway through the menstrual cycle. See how it happens.
Video: Baby's soft spots (fontanels)
A baby's soft spots (fontanels) close when the skull bones fuse together. See how.
X-linked agammaglobulinemia
This genetic disease weakens the immune system, mainly in males, and leads to having infections often.
Refine Your Search
Type
Gender
Age
- All
- 19 to 44 younger
- 45 to 64 middle
- 00 birth to 01 month newborn
- 02 months to 2 years infant/toddler
- 03 to 5 years preschool
- 13 to 18 years teen
- 06 to 12 years elementary/preteen
- 65 to 80 older
- 02 to 15 months infant
- 80 and over
- Premature baby
- 06 to 10 years elementary