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neurofibromatóza 1
Č. záznamu d009456 Dátum 06.06.2025 Typ M - MESH Tematický termín neurofibromatóza 1 Iný termín Angličtina (Pseudonym) Peripheral Neurofibromatosis
Angličtina (Pseudonym) Recklinghausen Disease of Nerve
Angličtina (Pseudonym) von Recklinghausen Disease
Slovenčina (Pseudonym) von Recklinghausenova choroba
Slovenčina (Pseudonym) neurofibromatóza periférna
Slovenčina (Pseudonym) Recklinghausenova choroba nervov
Pozri tiež (Skutočné meno) Noonanovej syndróm
(Skutočné meno) gény neurofibromatózy 1
(Skutočné meno) neurofibromín 1
(Skutočné meno) LEOPARD-syndróm
(Novšie záhlavie) Noonanovej syndróm
(Novšie záhlavie) gény neurofibromatózy 1
(Novšie záhlavie) neurofibromín 1
(Novšie záhlavie) LEOPARD-syndróm
MDT C04.557.580.600.580.590.650C04.700.631.650C10.562.600.500C10.574.500.549.400C10.668.829.675C16.320.400.560.400C16.320.700.633.650 Poznámka An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). 
predmetové heslo
Počet záznamov: 1