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| | Hereditary Coproporphyria |
 | | Hereditary coproporphyria shows itself in 2 ways, as "acute attacks" (see below) and as skin problems. | | | In hereditary coproporphyria the commonest situation is for neither skin problems nor acute attacks to occur, but either or both can occur in any one patient. | | | The name hereditary coproporphyria is used simply because it describes a laboratory finding in an inherited condition. |
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http://www.cpf-inc.ca/HCP.htm
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| | Encyclopedia |
| | Patients with variegate porphyria and hereditary coproporphyria patients may, in addition, experience cutaneous photosensitivity associated with the overproduction of porphyrins. | | | Patients with variegate porphyria or hereditary coproporphyria may, in addition, develop photosensitive skin lesions. | | | There is no specific treatment for the skin photosensitivity occurring in variegate porphyrin and hereditary coproporphyria, although &bgr;-carotene treatment has been suggested as useful. |
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http://www.eamg-med.com/members/encyclopedia/11/11_5.shtml
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| | Porphyria, Hereditary Coproporphyria |
| | Excess protoporphyrin is excreted by the liver into the bile, which in turn enters the intestine and is excreted in the feces. | | | Some patients develop skin photosensitivity, and must avoid sunlight. | | | The large amount of coproporphyrin present in Hereditary Coproporphyria (HCP) makes the patient sensitive to sunlight, but skin disease is rarely severe in this type or porphyria. |
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http://www.bchealthguide.org/kbase/nord/nord323.htm
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| | MedlinePlus: Porphyria |
| | Genetics Home Reference: Hereditary coproporphyria (National Library of Medicine) |
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http://www.nlm.nih.gov/medlineplus/porphyria.html
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| | Porphyria information |
| | If you have variegate porphyria or hereditary coproporphyria, your skin may also be affected. | | | In variegate porphyria, the skin changes and attacks of acute porphyria may not occur together at the same time. | | | Information for people with acute intermittent porphyria, variegate porphyria or hereditary coproporphyria and their families |
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http://www.cardiff.ac.uk/medicine/medical_biochem/porphyria/porphyria3.htm
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| | Hereditary coproporphyria - Genetics Home Reference |
| | In about 30 percent of people with hereditary coproporphyria, the skin is overly sensitive to sunlight. | | | Hereditary coproporphyria is a rare type of porphyria that can have acute (severe but usually not long-lasting) symptoms along with symptoms that affect the skin. | | | The signs and symptoms of hereditary coproporphyria are similar to those of acute intermittent porphyria, but attacks of acute symptoms tend to be less severe. |
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http://ghr.nlm.nih.gov/ghr/disease/hereditarycoproporphyria
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| | porphyria,Porphyria Cutanea Tarda,ALA-D Porphyria,Congenital Erythropoietic Porphyria,Hereditary Coproporphyria ... |
| | In patients with photosensitive skin changes alone, it is important to distinguish Varigate Porphyria or hereditary coproporphyria (HCP) from porphyria cutanea tarda (PCT), because treatment by phlebotomy or low-dose chloroquine is not successful in VP and HCP. | | | In hereditary coproporphyria, skin photosensitivity may also be a symptom. | | | acute intermittent porphyria, ALAD-deficiency porphyria, variegate porphyria, and hereditary coproporphyria |
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http://www.icomm.ca/geneinfo/porphyria.htm
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| | Porphyria |
| | The recoveries of porphyrins added to plasma were 71-114% except for protoporphyrin, which could not be reliably measured with this technique. | | | We studied 245 healthy subjects, 32 patients with classical porphyria cutanea tarda (PCT), 12 patients with PCT of renal failure, 13 patients with renal failure, 8 patients with pseudoporphyria of renal failure, 3 patients with acute intermittent porphyria, 5 patients with variegate porphyria, 5 patients with hereditary coproporphyria, and 4 patients with erythropoietic protoporphyria. | | | The dermatologist may play a key role in the early diagnosis of subclinical hereditary hemochromatosis in patients who present with porphyria cutanea tarda. |
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http://www.thedoctorsdoctor.com/diseases/porphyria.htm
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| | hereditary - OneLook Dictionary Search |
| | hereditary : Webster's 1828 Dictionary [ home, info ] | | | hereditary : ABTA Brain Tumor Patients [ home, info ] | | | hereditary : The On-line Medical Dictionary [ home, info ] |
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http://www.onelook.com/?w=hereditary&ls=a
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| | HEALTHMEDNET ILLNESS AND DISEASE URL DIRECTORY |
| | Hereditary peroneal nerve dysfunction see Charcot-Marie-Tooth disease (hereditary) Â Â Â Â Â Â Â Â Â Â | | | Hereditary Cancer Institute - Cancer Helpline [shc] Â Â Â Â Â Â Â Â Â Â Â | | | Hereditary Angioedema (90 sites / 100 books) Â Â Â Â |
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http://www.healthmednet.com/HERE-HIS.htm
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| | AllRefer Health - Porphyria (Acute Intermittent Porphyria, Congenital Erythropoietic Porphyria, Erythropoietic ... |
| | AllRefer Health - Porphyria (Acute Intermittent Porphyria, Congenital Erythropoietic Porphyria, Erythropoietic Protoporphyria, Hereditary Coproporphyria) | | | Alternate Names : Acute Intermittent Porphyria, Congenital Erythropoietic Porphyria, Erythropoietic Protoporphyria, Hereditary Coproporphyria | | | Porphyria is a group of inherited disorders involving abnormalities in the production of heme pigments (the base material responsible for hemoglobin (red blood cell pigment), myoglobin (reddish muscle cell pigment) and another group of materials called cytochromes. |
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http://health.allrefer.com/health/porphyria-info.html
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| | Disease Reference |
| | The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. | | | Hereditary sensory and autonomic neuropathy - type III |
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http://www.healthscout.com/ency/index/diseidxh.htm
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| | Porphyria hereditary coproporphyria - Wikipedia, the free encyclopedia |
| | Search for Porphyria hereditary coproporphyria in other articles | | | Look for Porphyria hereditary coproporphyria in Wiktionary, our sister dictionary project. | | | If you created an article under this title previously, it may have been deleted. |
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http://en.wikipedia.org/wiki/Porphyria__hereditary_coproporphyria
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| | Porphyria / Hereditary Coproporphyria |
| | HCP is characterized primarily by neurovisceral symptoms as seen in acute intermittent porphyria (AIP); however, approximately 30% have photosensitivity similar to that seen in porphyria cutanea tarda (PCT). | | | — Hereditary coproporphyria (HCP) tends to be latent before puberty, with symptoms being more common in adult women than adult men. | | | Increased production of porphobilinogen (PBG) and delta-aminolevulinic acid (ALA) are associated with neurovisceral complaints, while increased production of porphyrins cause photosensitization. |
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http://intmedweb.wfubmc.edu/blurbs/ho/porphyria.html
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| | hereditary coproporphyria - General Practice Notebook |
| | Oxbridge Solutions Ltd® is an independent company owned by the authors which does not receive income from any other organisation or individual. | | | It is very rare and may present at any age. | | | Hereditary coproporphyria is an autosomal dominant deficiency of coproporphyrinogen oxidase (chromosome 9) in white blood cells, liver and other cells. |
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http://www.gpnotebook.com/cache/1637482504.htm
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| | Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism -- Takeuchi et al. 98 (13): 3871 -- Blood |
| | Hereditary coproporphyria (HCP) is a hereditary autosomal-dominant disease of heme biosynthesis resulting from a partial deficiency | | | From Department of Pediatrics and the Department of Pediatric Urology, Nagoya Daini Red Cross Hospital, Japan; the Department of Nutrition and Biochemistry, National Institute of Public Health, Tokyo, Japan; the Third Department of Internal Medicine, Yamagata University School of Medicine, Japan; and the Department of Pediatrics, Nagoya City University, Japan. | | | Harderoporphyria, a rare erythropoietic variant form of HCP, is |
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http://www.bloodjournal.org/cgi/content/full/98/13/3871
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| | Porphyria hereditary coproporphyria - Wiktionary |
| | Wiktionary does not have an entry for this word yet. | | | If you created an entry under this title previously, it may have been deleted. |
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http://en.wiktionary.org/wiki/:Porphyria_hereditary_coproporphyria
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| | CPOX - Genetics Home Reference |
| | At least 34 mutations that cause hereditary coproporphyria and the more severe form of the disorder, harderoporphyria, have been identified in the CPOX gene. | | | One mutation, a substitution of the amino acid glutamic acid for lysine at position 404 (also written as Lys404Glu or K404E), has been found in all families with harderoporphyria. | | | hereditary coproporphyria - caused by mutations in the CPOX gene |
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http://ghr.nlm.nih.gov/ghr/gene/cpo/aspect/GeneDBs
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| | Encyclopedia Search - Medical Dictionary Search Engines |
| | Abnormal uterine bleeding see Vaginal bleeding between periods | | | ABPA see Pulmonary aspergillosis - allergic bronchopulmonary type | | | Abnormality of the urea cycle - hereditary see Hereditary urea cycle abnormality |
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http://medical-dictionary-search-engines.com/encyclopedia/?encyclopedia_name...
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