Search Results 21-30 of 17117 for waardenburg syndrome
Your child's healthcare professional may suspect Angelman syndrome if your child has developmental delays, talks little or not at all, or has other symptoms.
In this condition, a genetic male has an extra X sex chromosome. This may affect the growth of testicles and result in low testosterone.
Learn about the symptoms, causes and treatments for this heart rhythm condition that is sometimes inherited.
Hirschsprung (HIRSH-sproong) disease is a condition in which nerve cells are missing in a baby's large intestine, resulting in bowel blockage.
Learn about these complex genetic conditions that cause problems with connective tissue in the skin, joints and blood vessel walls.
Some short-term studies in adults with growth hormone deficiency also show that they benefit lean body mass and also muscle tone. Another big endocrine disorder ...
Diagnosis. Typically, healthcare professionals suspect Prader-Willi syndrome based on symptoms. A diagnosis can be made through genetic testing nearly all ...
Each Mayo Clinic location offers care for adults with congenital heart disease. At Mayo Clinic's campus in Minnesota, healthcare professionals in the Center for ...
Prader-Willi syndrome is a genetic condition associated with cognitive and behavioral symptoms, delays in development, chronic hunger, and low levels of ...
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive ciliopathy characterized by multisystem involvement, including early-onset hyperphagia and obesity, ...
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