| Health / Medical Topics |
Infantile Neuronal Ceroid Lipofuscinosis
A very rare form of neuronal ceroid lipofuscinosis inherited in an autosomal recessive pattern. During the first six to eighteen months of life development is normal. Subsequently, patients develop developmental abnormalities in speech and motor skills, blindness, epilepsy, and seizures. (NCI Thesaurus)
YOU MAY ALSO LIKE
A rare autosomal recessive neurodegenerative disorder caused by mutations in the PLA2G6 gene. It is characterized by the development of swellings called…
A rare condition in which one or more fibrous (connective tissue) tumors form in the skin, muscle, or bone. Sometimes, they also…
A rare type of soft tissue tumor that begins in cells that wrap around blood vessels. Infantile hemangiopericytomas may be benign (not…
A capillary hemangioma that may regress spontaneously. It occurs in infants and children.
An inherited disorder in which there is a lower-than-normal number of neutrophils (a type of white blood cell that is important in…
Effortless regurgitation of food, milk, and saliva that commonly occurs in infants, usually right after feeding or burping.
