Variegate porphyria (VP) is an autosomal dominant condition that results from the deficiency of protoporphyrinogen oxidase (PPOX, EC 1.3). The build-up of porphyrin precursors delta-aminolevulinic ...

This page lists all known medications that could potentially lead to 'Variegate porphyria' as a side effect. It's important to note that mild side effects are quite common with medications. The ...

Haemoglobin is protein found in red blood cells that carries oxygen, it also gives the red color. Now how is it related to the genetic disorder like Porphyria? Porphyria is a group of rare genetic ...

Dublin, Nov. 15, 2021 (GLOBE NEWSWIRE) -- The "Porphyria: Pipeline Review, Developer Landscape and Competitive Insights, 2021-2031" report has been added to ResearchAndMarkets.com's offering. This ...

Wilmington, Delaware, United States, Transparency Market Research Inc. -, Aug. 27, 2024 (GLOBE NEWSWIRE) -- The global acute intermittent porphyria market (급성 간헐성 포르피린증 시장) is estimated to surge at a ...

Acute porphyrias are rare genetic disorders that present with neurologic and systemic symptoms, including abdominal pain, hyponatremia and seizures. When porphyria is suspected, a urine screening ...

Most of the porphyrias are inherited conditions. The genes for all the enzymes in the heme pathway have been identified. Some forms of porphyria result from inheriting one altered gene from one parent ...

The madness of King George III has been attributed to acute intermittent porphyria, an inherited genetic disorder of the heme biosynthesis pathway. Acute attacks of porphyria result in ...

Figure 1: Clinical and biochemical analyses of rare variant alleles of ABCB6 in porphyric patients. There was minimal or no difference in translation of the WT or ABCB6 variants (Supplementary Fig. 2a ...

Porphyria cutanea tarda (PCT) is a common form of hepatic porphyria characterized by symptoms such as fragile, blister-prone skin particularly on sun-exposed areas. The condition occurs due to an ...