Maple syrup urine disease
Maple syrup urine disease (MSUD) is a genetic medical disorder. It causes a problem with how the human body deals with amino acids. It is also called branched chain ketoaciduria. Maple syrup urine disease affects about 1 in 185,000 infants worldwide.
The most noticeable symptom of the disorder is an infant with sweet-smelling urine. Infants with this disease seem healthy at birth. If the disease is not treated, the person will suffer severe brain damage and eventually die. MSUD is much more common in children of Amish and Mennonite descent.[source?]
From a very early age, the condition can be recognised by poor feeding, vomiting, lack of energy, seizures, and mental health issues. The urine of infants with this disease has a very sweet odor, much like burned caramel or maple syrup. This is what gives the condition its name.
Maple Syrup Urine Disease Media
Maple syrup urine disease has an autosomal recessive pattern of inheritance.