טוען...
Sporadic Porphyria Cutanea Tarda as the Initial Manifestation of Hereditary Hemochromatosis
Porphyria cutanea tarda (PCT) is a skin disorder characterized by abnormal heme synthesis. We present a 45-year-old man with intermittent skin lesions recurring annually for years. Skin biopsy and measurement of serum heme precursors confirmed a diagnosis of PCT. He had persistently elevated alanine...
שמור ב:
| הוצא לאור ב: | ACG Case Rep J |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Wolters Kluwer
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7145215/ https://ncbi.nlm.nih.gov/pubmed/32309465 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14309/crj.0000000000000247 |
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