AI Article Synopsis

  • Porphyria is a rare group of genetic or acquired disorders caused by enzyme deficiencies in the hemoglobin biosynthetic pathway, leading to various symptoms.
  • The case study focuses on a seven-year-old girl with severe symptoms including muscle weakness, high blood pressure, abdominal pain, and seizures, complicating the diagnosis due to their rarity.
  • Her diagnosis of Acute Intermittent Porphyria (AIP) was confirmed by a positive urinary porphobilinogen test, demonstrating the need for prompt recognition and management of this condition.

Article Abstract

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.

Download full-text PDF

Source
http://dx.doi.org/10.47391/JPMA.7390DOI Listing

Publication Analysis

Top Keywords

quadriparesis hypertension
8
hypertension recurrent
8
recurrent severe
8
severe cyclic
8
cyclic abdominal
8
abdominal pain
8
pain seizures
8
acute porphyria
4
porphyria unusual
4
unusual case
4

Similar Publications

Article Synopsis
  • * Despite successful mechanical thrombectomy (MT) and stenting achieving full recanalization, the patient showed poor recovery in hearing, with persistent bilateral SNHL remaining post-treatment.
  • * The study underscores the complexity of neurological outcomes after vertebrobasilar occlusion, suggesting that while MT might alleviate other neurologic symptoms, its effectiveness on SNHL can vary greatly among patients.
View Article and Find Full Text PDF

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 PDF

Heart-Shaped Infarct on MRI and Its Implications in Bilateral Medullary Syndrome.

Cureus

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 PDF

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 PDF

Tumefactive 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.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!