Deficiency, UROD


Deficiency, UROD
Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light-sensitive) skin disease with onset in adult life with a large amount of a substance called uroporphyrin in the urine. UROD is an enzyme required for the synthesis of heme (part of hemoglobin, the pigment in red blood cells that carries oxygen). The hallmarks of porphyria cutanea tarda (PCT) are blisters which become ulcerated in areas of the skin exposed to sunlight, especially on the face, ears and dorsum (back) of the hands. The affected areas of skin also tend to be fragile and show hyperpigmentation (excess pigment) and hypertrichosis (excess hair). PCT, the most common form of porphyria, comes in two clinical familial and a sporadic form: {{}}The familial form of PCT — is inherited as an autosomal dominant trait with males and females affected in multiple generations. The enzyme UROD is reduced in all tissues. The sporadic form of PCT — is more common. The enzyme UROD is only reduced in the liver. It appears sporadically in people with liver disease, as from alcoholism, and from exposure to agents such as estrogens. Iron overload is frequently present in PCT and may be associated with varying degrees of damage of the liver. A severe form of PCT, hepatoerythropoietic porphyria (HEP), has its onset in infancy with the accumulation of protoporphyrin in the red blood cells. The level of the enzyme UROD is very low in red cells. The UROD gene has been mapped to 1p34. Mutations have been identified in the UROD gene, including DNA base substitutions and deletions. These mutations result in reduced activity of the enzyme. Some mutation result in PCT and others in the recessively inherited HEP. HEP is the homozygous form of familial PCT. Treatment is directed first at reducing iron overload by regular phlebotomy (removal of blood). Then treatment with the drug chloroquine usually induces rapid remission that is sustained while chloroquine is continued in regular low doses.

Medical dictionary. 2011.

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  • UROD deficiency — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… …   Medical dictionary

  • Deficiency, uroporphyrinogen decarboxylase — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… …   Medical dictionary

  • Uroporphyrinogen decarboxylase deficiency — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… …   Medical dictionary

  • Porphyria cutanea tarda — DiseaseDisorder infobox Name = Porphyria cutanea tarda Caption = Porphyria cutanea tarda on the hands ICD10 = ICD10|E|80|1|e|70 ICD9 = ICD9|277.1 Porphyria cutanea tarda (PCT) is the most common subtype of porphyria. The disorder results from low …   Wikipedia

  • Porphyria cutanea tarda — Literally, the late skin form of porphyria, a genetic photosensitive (light sensitive) skin disease with onset in adult life with substances called uroporphyrins in the urine due to a deficiency of uroporphyrinogen decarboxylase (UROD), an enzyme …   Medical dictionary

  • 1-я хромосома человека — Идиограмма 1 й хромосомы человека 1 я хромосома человека  самая большая из 23 человеческих хромосом, одна из 22 аутосом человека. Хромосома содержит около 248 млн пар оснований …   Википедия

  • PCT — The abbreviation PCT stands for a number of things including porphyria cutanea tarda, literally, the late skin form of porphyria, a genetic photosensitive (light sensitive) skin disease with onset in adult life with substances called… …   Medical dictionary

  • Uroporphyrinogen III decarboxylase — Uroporphyrinogen decarboxylase, also known as UROD, is a human gene.cite web | title = Entrez Gene: UROD uroporphyrinogen decarboxylase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7389| accessdate = ]… …   Wikipedia

  • Chromosome 1 (human) — Map of Chromosome 1 Chromosome 1 is the designation for the largest human chromosome. Humans have two copies of chromosome 1, as they do with all of the autosomes, which are the non sex chromosomes. Chromosome 1 spans about 247 million nucleotide …   Wikipedia

  • Heme — A heme (American English) or haem (British English) is a prosthetic group that consists of an iron atom contained in the center of a large heterocyclic organic ring called a porphyrin . Not all porphyrins contain iron, but a substantial fraction… …   Wikipedia


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