Health / Medical Topics

    Cri du Chat Syndrome

    A genetic syndrome resulting from a partial deletion on the short arm of chromosome 5. It is characterized by a cat-like cry in infancy, microcephaly, mental retardation, growth failure, round face, hypertelorism, and cardiac failure. (NCI Thesaurus)




    YOU MAY ALSO LIKE

    CRHR1 wt Allele
    Human CRHR1 wild-type allele is located within 17q12-q22 and is approximately 52 kb in length. This allele, which encodes corticotropin-releasing factor receptor…
    CRHR1 Gene
    This gene is involved in hormone recognition.
    CRH wt Allele
    Human CRH wild-type allele is located in the vicinity of 8q13 and is approximately 2 kb in length. This allele, which encodes…
    CRH Gene
    This gene plays a role in several metabolic functions and is involved in the stimulation of parturition.
    Creutzfeldt-Jakob Disease
    A rare transmittable degenerative disorder of the brain caused by prions. Morphologically it is characterized by spongiform degeneration of the cerebral and…
    Crestor
    A drug used to lower the amount of cholesterol and other harmful substances, such as triglycerides, in the blood. It is also…

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact