A World of Knowledge
    Health / Medical Topics

    Infantile Refsum Disease

    A genetic disorder characterized by abnormalities in the breakdown of phytanic acid. It results in accumulation of phytanic acid in the blood, brain and other tissues. Signs and symptoms include retinitis pigmentosa which may lead to blindness, hearing problems and deafness, hypotonia, ataxia, nystagmus, facial deformities, and mental and growth retardation. (NCI Thesaurus)




    YOU MAY ALSO LIKE

    A very rare form of neuronal ceroid lipofuscinosis inherited in an autosomal recessive pattern. During the first six to eighteen months of…
    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…

    © 1991-2024 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact