The following Conditions are related to Hypotonia
Select a specific condition below to view its details.
- Cps deficiency
Carbamoyl phosphate synthetase 1 CPS deficiency is a genetic disease that is passed down hereditarily, and hence there is always a risk that if your ancestors had it, you or your children could have it.When a gene is autosomal, it can be found on any chromosome other than the X or Y chromosomes (sex chromosomes).Like chromosomes, genes frequently exist in pairs.Recessive means that for a person to Read More
- Lcad deficiency
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that restricts the body from converting specific fats to energy, especially during periods of fasting.The symptoms of LCAD deficiency appear during infancy or early childhood.It involves hypoglycemia (low blood sugar), lethargy (lack of energy) and muscle weakness.The individuals who are affected by this disorder are also hig Read More