Galactosemia
| Galactosemia | |
|---|---|
| Specialty | Endocrinology  |
Galactosemia is a rare genetic metabolic disorder which affects an individual's ability to properly metabolize the sugar galactose.
Goppert first described the disease in 1917,[1] with its cause as a defect in galactose metabolism being identified by a group led by Herman Kalckar in 1956.[2]
Its incidence is about 1 per 47,000 births (classic type). It is much rarer in Japan and much more common in Italy, specifically the traveler region. Galactosaemia is also very common within the Irish Traveller population. This is attributed to consanguinity within a relatively small gene pool.
Cause
Lactose in food (such as dairy products) is broken down by the body into glucose and galactose.
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In individuals with galactosemia, the enzymes needed for further metabolism of galactose are severely diminished or missing entirely, leading to toxic levels of galactose to build up in the blood, resulting in hepatomegaly (an enlarged liver), renal failure, cataracts, and brain damage. Without treatment, mortality in infants with galactosemia is about 75%.
The 4th carbon on Galactose has an axial hydroxyl (-OH) group. This causes Galactose to favor the open form as it is more stable than the closed form. This leaves an aldehyde (O=CH-) group available to react with nucleophiles, particularly proteins which contain amino (-NH2) groups, in the body. This uncontrolled reactivity gives way to glycolation. Glycolation causes disease by altering the structure of proteins in ways that were not intended for biochemical processes.
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Axial hydroxyl group drawn in red.
Types
Galactose is converted into glucose by the action of three enzymes, known as the Leloir pathway. Accordingly, there are 3 known types of Galactosemia; type 1, 2 and 3:
| Type | Diseases Database | OMIM | Gene | Locus | Enzyme | Name |
| Type 1 | Template:DiseasesDB2 | Template:OMIM2 | GALT | 9p13 | galactose-1-phosphate uridyl transferase | classic galactosemia |
| Type 2 | Template:DiseasesDB2 | Template:OMIM2 | GALK1 | 17q24 | galactokinase | galactokinase deficiency |
| Type 3 | Template:DiseasesDB2 | Template:OMIM2 | GALE | 1p36-p35 | UDP galactose epimerase | galactose epimerase deficiency, UDP-Galactose-4-epimerase deficiency |
The order of these three types is not the same as the order that the enzymes are encountered by galactose on its metabolic path (which is closer to GALK, GALT, and then GALE, though many variations can occur.)
Diagnosis
Infants are now routinely screened for galactosemia in the United States, and the diagnosis is made while the person is still an infant.
Treatment
The only treatment for classic galactosemia is eliminating lactose and galactose from the diet. Even with an early diagnosis and a restricted diet, however, some individuals with galactosemia experience long-term complications such as speech difficulties, learning disabilities, neurological impairment (e.g. tremors, etc), and in girls, ovarian failure. These complications are treated if they appear in a manner similar to the way they would be treated in a non-galactosemic. Such complications have not been associated with Duarte galactosemia, and many individuals with Duarte galactosemia do not need to restrict their diet at all. Infants with classic galactosemia cannot be breast-fed due to lactose in human breast milk and are usually fed a soy-based formula.[3]
Galactosemia is sometimes confused with lactose intolerance, but galactosemia is a more serious condition. Lactose intolerant individuals have an acquired or inherited shortage of the enzyme lactase, and experience abdominal pains after ingesting dairy products, but no long-term effects. In contrast, a galactosemic individual who consumes galactose can cause permanent damage to their bodies.
Long term complication of galactosemia includes:
- Speech deficits
- Ataxia
- Dysmetria
- Diminished bone density
- Premature ovarian failure
- Cataract
For a thorough scientific overview of galactosemia, one can consult chapter 72 of OMMBID[4]. For more online resources and references, see inborn error of metabolism.
References
- ^ Goppert F. Galaktosurie nach Milchzuckergabe bei angeborenem, familiaerem chronischem Leberleiden. Klin Wschr 1917;54:473-477.
- ^ Isselbacher KJ, Anderson EP, Kurahashi K, Kalckar HM (1956). "Congenital galactosemia, a single enzymatic block in galactose metabolism". Science. 13 (123): 635–6. PMID 13311516.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ http://www.cdc.gov/breastfeeding/disease/contraindicators.htm
- ^ Charles Scriver, Beaudet, A.L., Valle, D., Sly, W.S., Vogelstein, B., Childs, B., Kinzler, K.W. (2006). The Online Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill. - Free summaries of 255 chapters, full text through many universities and organizations. Also, the OMMBID blog.
External links
- Galactosemia Resources and Information
- Parents of Galactosemic Children, Inc. website
- What is Galactosemia?
- Galactosemic Families of Minnesota
- Galactosemia Handbook - A Guide for Families
Template:Endocrine, nutritional and metabolic pathology
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