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progéria
Č. záznamu d011371 Dátum 06.06.2025 Typ M - MESH Tematický termín progéria Iný termín Angličtina (Pseudonym) Hutchinson-Gilford Syndrome
Slovenčina (Pseudonym) Hutchinsonov-Gilfordov syndróm
Slovenčina (Pseudonym) nanizmus senilný
Pozri tiež (Skutočné meno) Cockayneov syndróm
(Skutočné meno) Wernerov syndróm
MDT C16.320.488.875C16.320.565.753C18.452.648.753 Poznámka An 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. 
predmetové heslo
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