Number of the records: 1  

progéria

  1. Record numberd011371
    Date06.06.2025
    TypeM
    Topical termprogéria
    Other termEnglish (Pseudonym) Hutchinson-Gilford Syndrome
    Slovak (Pseudonym) Hutchinsonov-Gilfordov syndróm
    Slovak (Pseudonym) nanizmus senilný
    See also(Skutočné meno) Cockayneov syndróm
    (Skutočné meno) Wernerov syndróm
    UDCC16.320.488.875C16.320.565.753C18.452.648.753
    NoteAn abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA.
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Number of the records: 1  

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