Porphyria: varied ocular manifestations and management

Sati, Alok; Sangwan, Virender S.; Basu, Sayan
May 2013
BMJ Case Reports;May2013, p1
Academic Journal
No abstract available.


Related Articles

  • Diagnosis and management of porphyria. Thadani, Helen // BMJ: British Medical Journal (International Edition);06/17/2000, Vol. 320 Issue 7250, p1647 

    Discusses the diagnosis and clinical management of neuropsychiatric porphyria. Medical information on porphyria; General clinical aspects of porphyria; Acute attacks of porphyria.

  • Neuropathic pain in hereditary coproporphyria. Guan-Liang Chen; Deng-Ho Yang; Jeng-Yuau Wu; Chia-Wen Kuo; Wen-Hsiu Hsu // Pakistan Journal of Medical Sciences;Apr2013, Vol. 29 Issue 2, p672 

    Acute porphyrias are rare diseases with varying incidences worldwide. These diseases are disorders of heme biosynthesis characterized by acute attacks of neurological symptoms. Acute porphyria should be considered in patients with unexplained abdominal pain or neurological damage. Clinical...

  • Shared care approach to managing ophthalmological disease in patients with positive treponemal serology: a case series. Karunaratne, I.; Sharma, S.; Dick, A.; Carrington, D.; Homer, P. // International Journal of STD & AIDS;Apr2012, Vol. 23 Issue 4, p291 

    Ocular syphilis presenting initially as various manifestations of intraocular inflammation is a rare but an important manifestation of syphilis. Ocular phenotypes are varied and mimic other infectious and non-infectious ocular diseases. Uncertainties exist in optimal management of ocular...

  • THE CLINICAL SIGNIFICANCE OF ACUTE PORPHYRIA. Redeker, Allan G. // American Journal of Gastroenterology;Mar1956, Vol. 25 Issue 3, p266 

    Looks into the clinical significance of acute porphyria as a diagnostic and therapeutic indicators in various diseases. Diagnosis; Manifestations of porphyria; Assessment of the various cases of porphyria.

  • Post Partum Acute Intermittent Porphyria: A Case Report. Gaurav, Tomar; Sethi, Ashish; Kriplani, T. C.; Narang, Neeraj // Indian Anaesthetists' Forum;2010, Special section p1 

    Porphyrias are inherited disorders, each involving a specific enzyme in heme biosynthetic pathways. These are classified as hepatic or erythropoietic depending on the primary site of overproduction and accumulation of porphyrin. Hepatic porphyria manifested with neurological sign & symptoms...

  • Porphyria cutanea tarda and HIV/AIDS: a review of pathogenesis, clinical manifestations and management. Mansourati, Fadi F.; Stone, Valerie E.; Mayer, Kenneth H. // International Journal of STD & AIDS;Jan1999, Vol. 10 Issue 1, p51 

    The porphyrias, a group of rare acquired or hereditary diseases, are due to abnormalities in the haeme biosynthesis pathway. Clinical manifestations vary with the deficient enzyme. Porphyria cutanea tarda (PCT), the most common of the porphyrias, is the result of decreased function of the enzyme...

  • Variegate Porphyria. Mustajoki, Pertti // Annals of Internal Medicine;Aug78, Vol. 89 Issue 2, p238 

    Deals with a study which dealt with the diagnosis of a patient with variegate porphyria. Clinical manifestations of the disease; Similarities of variegate porphyria with other hereditary hepatic porphyrias; Skin manifestations associated with the disease.

  • Intensive care management of patients with acute intermittent porphyria: Clinical report of four cases and review of literature. Mehta, Madhur; Rath, Girija P.; Padhy, Uma P.; Marda, Manish; Mahajan, Charu; Dash, Hari H. // Indian Journal of Critical Care Medicine;Apr-Jun2010, Vol. 14 Issue 2, p88 

    Acute intermittent porphyria (AIP), the most common and the most severe form of acute hepatic porphyria, is an autosomal dominant condition. It results from lower-than-normal levels (less than 50%) of porphobilinogen (PBG) deaminase. Patients may present commonly with gastrointestinal complaints...

  • Acute intermittent porphyria presenting as epilepsy. Scane, Andrew C.; Wight, Jeremy P.; Godwin-Austen, Richard B. // British Medical Journal (Clinical Research Edition);4/5/1986, Vol. 292 Issue 6525, p946 

    Presents a case report on the failure to recognize porphyria as the cause of motor polyneuropathy. Characteristics of porphyria; Increase of porphobilinogen and free porphyrins in the urine; Manifestations of the disease.

  • European Porphyria Initiative (EPI): A Platform to Develop a Common Approach to the Management of Porphyrias and to Promote Research in the Field. Deybach, J.-Ch.; Badminton, M.; Puy, H.; Sandberg, S.; Frank, J.; Harper, P.; Martasek, P.; Minder, E.; Parker, S.; Thunell, S.; Elder, G. // Physiological Research;2006 Supplement, Vol. 55, pS67 

    Porphyrias are uncommon inherited diseases of haem biosynthesis for which the diagnosis and treatment varies in individual countries. Despite the existence of guidelines recommended by porphyria experts concerning the diagnosis and management of the acute porphyrias, and of specialist centres in...


Read the Article


Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics