Porphyria refers to a rare group of genetically inherited or acquired disorders that arise due to reduced metabolic activity of any of the enzymes in the haem biosynthetic pathway. Defect in any enzyme causes the presentation of symptoms of porphyria. The epidemiology of Acute Intermittent Porphyria (AIP) is complicated because of its rarity and delay in diagnosis. We present the case of a seven-year-old girl who presented with multisystem involvement; her symptoms were quadriparesis, hypertension, recurrent severe cyclic abdominal pain, and seizures. These symptoms together were not explained by the differentials taken into account. She presented before puberty with no family history of such conditions, while being born of consanguineous marriage. Her symptoms along with urinary porphobilinogen positivity test helped to reach the diagnosis of AIP in the absence of cutaneous manifestations. This case highlights the variable presentation of porphyria and emphasises the importance of appropriate and timely diagnosis and management in these patients.
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http://dx.doi.org/10.47391/JPMA.7390 | DOI Listing |
Neuroradiol J
December 2024
Department of Neurology, Istanbul Aydin University, Istanbul, Turkey.
Cureus
October 2024
Department of Neuroscience, Instituto Nacional de Cancerología, Mexico City, MEX.
Wallenberg syndrome, also known as lateral medullary syndrome, is a rare condition affecting the vertebrobasilar circulation, causing symptoms such as vertigo, nystagmus, dysarthria, and hemifacial weakness. Typically linked to ischemic strokes, it can also arise from vertebrobasilar aneurysms. In rare cases, subclavian steal syndrome (SSS), involving retrograde flow in the vertebral artery due to subclavian stenosis, complicates the picture, as observed in this case of a 66-year-old woman with both conditions and a vertebrobasilar aneurysm.
View Article and Find Full Text PDFCureus
September 2024
Internal Medicine, Saveetha Medical College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.
Bilateral medullary syndrome (BMS) is an extremely rare and devastating neurological disorder resulting from ischemia or infarction of the medulla oblongata. This case report presents two unique instances of BMS, both leading to fatal outcomes. Case 1 describes a 70-year-old male with a history of systemic hypertension who presented with limb weakness, slurred speech, and dysphagia.
View Article and Find Full Text PDFHeliyon
August 2024
Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Anterior spinal artery occlusion resulting in bilateral medial medullary infarction (bMMI) and anterior spinal artery syndrome (ASAS) simultaneously has been rarely described. To the best of our knowledge, this is the first report of such occurrence during pregnancy. A 23-year-old preeclamptic parturient at 37 weeks underwent an emergent cesarean section after developing gradual neurological deficits.
View Article and Find Full Text PDFTumefactive demyelinating lesions remain a rare entity and a source of diagnostic difficulty. Here, we report the case of a teenage girl who presented with a one-month history of progressive quadriparesis and symptoms of intracranial hypertension. Brain MRI showed multiple large subcortical white matter lesions with both open- and closed-rim enhancement on gadolinium injection.
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