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Acute Intermittent Porphyria Labeled Initially As Guillain-Barre Syndrome: Challenging Diagnosis.
Alayafi, Hassan A; Aljumah, Talal K; Alluhayyan, Omar B; Alqaraishi, Ali; Aljwair, Sarah A.
Affiliation
  • Alayafi HA; Neurology, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Research Center, King Abdullah International Medical Research Centre, Riyadh, SAU.
  • Aljumah TK; Neurology, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Research Center, King Abdullah International Medical Research Centre, Riyadh, SAU.
  • Alluhayyan OB; Internal Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Research Center, King Abdullah International Medical Research Centre, Riyadh, SAU.
  • Alqaraishi A; Internal Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Research Center, King Abdullah International Medical Research Centre, Riyadh, SAU.
  • Aljwair SA; Neurology, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Research Center, King Abdullah International Medical Research Centre, Riyadh, SAU.
Cureus ; 15(11): e48753, 2023 Nov.
Article in En | MEDLINE | ID: mdl-38094544
Acute intermittent porphyria (AIP) is an autosomal, dominant, rare metabolic disturbance that results from a defect in the activity of the heme biosynthesis. It has a heterogeneous presentation, making a prompt diagnosis challenging. We report a case of acute intermittent porphyria in a young female who underwent in vitro fertilization (IVF) and presented with recurrent abdominal pain and posterior reversible encephalopathy syndrome (PRES), progressing to acute progressive quadriparesis post-delivery.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cureus Year: 2023 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cureus Year: 2023 Document type: Article Country of publication: United States