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porfýrie hepatálne
Č. záznamu d017094 Dátum 06.06.2025 Typ M - MESH Tematický termín porfýrie hepatálne Iný termín Angličtina (Pseudonym) Hepatic Porphyria
Slovenčina (Pseudonym) porfýria hepatická
Slovenčina (Pseudonym) porfýria hepatálna
Slovenčina (Pseudonym) porfýria pečene
Slovenčina (Pseudonym) porphyriae hepaticae
MDT C06.552.830C16.320.850.742C17.800.827.742C18.452.811.400 Poznámka A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues. predmetové heslo
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