Hexokinase deficiency: Difference between revisions
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{{Infobox medical condition | |||
| name = Hexokinase deficiency | |||
| image = [[File:Autosomal_recessive_-_en.svg|200px]] | |||
| caption = Hexokinase deficiency is inherited in an [[autosomal recessive]] pattern. | |||
| field = [[Hematology]] | |||
| symptoms = [[Hemolytic anemia]], [[fatigue]], [[jaundice]], [[splenomegaly]] | |||
| complications = [[Gallstones]], [[iron overload]] | |||
| onset = Usually in [[infancy]] or [[childhood]] | |||
| duration = Lifelong | |||
| causes = Mutations in the [[HK1 gene]] | |||
| risks = Family history of the condition | |||
| diagnosis = [[Blood test]], [[genetic testing]] | |||
| differential = [[Pyruvate kinase deficiency]], [[G6PD deficiency]] | |||
| treatment = [[Blood transfusion]], [[splenectomy]] | |||
| medication = [[Folic acid]] supplementation | |||
| prognosis = Variable, depending on severity | |||
| frequency = Rare | |||
}} | |||
'''Hexokinase deficiency''' is a rare [[genetic disorder]] that affects the body's ability to metabolize glucose, leading to a variety of symptoms including [[anemia]], [[jaundice]], and [[fatigue]]. This condition is caused by mutations in the HK1 gene, which provides instructions for making an enzyme called hexokinase. | '''Hexokinase deficiency''' is a rare [[genetic disorder]] that affects the body's ability to metabolize glucose, leading to a variety of symptoms including [[anemia]], [[jaundice]], and [[fatigue]]. This condition is caused by mutations in the HK1 gene, which provides instructions for making an enzyme called hexokinase. | ||
==Causes== | ==Causes== | ||
Hexokinase deficiency is caused by mutations in the [[HK1 gene]]. This gene provides instructions for making an enzyme called hexokinase, which plays a crucial role in the first step of glucose metabolism. Mutations in the HK1 gene reduce the activity of hexokinase, disrupting the normal process of glucose metabolism and leading to the symptoms of hexokinase deficiency. | Hexokinase deficiency is caused by mutations in the [[HK1 gene]]. This gene provides instructions for making an enzyme called hexokinase, which plays a crucial role in the first step of glucose metabolism. Mutations in the HK1 gene reduce the activity of hexokinase, disrupting the normal process of glucose metabolism and leading to the symptoms of hexokinase deficiency. | ||
==Symptoms== | ==Symptoms== | ||
The symptoms of hexokinase deficiency can vary widely, but they often include: | The symptoms of hexokinase deficiency can vary widely, but they often include: | ||
* [[Anemia]]: A condition characterized by a lack of healthy red blood cells, leading to fatigue and weakness. | * [[Anemia]]: A condition characterized by a lack of healthy red blood cells, leading to fatigue and weakness. | ||
* [[Jaundice]]: A yellowing of the skin and eyes, caused by a buildup of a substance called bilirubin. | * [[Jaundice]]: A yellowing of the skin and eyes, caused by a buildup of a substance called bilirubin. | ||
* [[Fatigue]]: A feeling of tiredness or exhaustion that doesn't go away with rest. | * [[Fatigue]]: A feeling of tiredness or exhaustion that doesn't go away with rest. | ||
==Diagnosis== | ==Diagnosis== | ||
Diagnosis of hexokinase deficiency typically involves a series of tests, including blood tests to check for anemia and jaundice, and genetic testing to identify mutations in the HK1 gene. | Diagnosis of hexokinase deficiency typically involves a series of tests, including blood tests to check for anemia and jaundice, and genetic testing to identify mutations in the HK1 gene. | ||
==Treatment== | ==Treatment== | ||
Treatment for hexokinase deficiency is typically focused on managing the symptoms of the condition. This can include treatments for anemia and jaundice, as well as lifestyle changes to help manage fatigue. | Treatment for hexokinase deficiency is typically focused on managing the symptoms of the condition. This can include treatments for anemia and jaundice, as well as lifestyle changes to help manage fatigue. | ||
==See also== | ==See also== | ||
* [[Glucose metabolism]] | * [[Glucose metabolism]] | ||
* [[Genetic disorders]] | * [[Genetic disorders]] | ||
* [[HK1 gene]] | * [[HK1 gene]] | ||
==References== | ==References== | ||
<references /> | <references /> | ||
{{stub}} | {{stub}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Metabolic disorders]] | [[Category:Metabolic disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
Latest revision as of 02:48, 6 April 2025
Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC
| Hexokinase deficiency | |
|---|---|
| |
| Synonyms | N/A |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Hemolytic anemia, fatigue, jaundice, splenomegaly |
| Complications | Gallstones, iron overload |
| Onset | Usually in infancy or childhood |
| Duration | Lifelong |
| Types | N/A |
| Causes | Mutations in the HK1 gene |
| Risks | Family history of the condition |
| Diagnosis | Blood test, genetic testing |
| Differential diagnosis | Pyruvate kinase deficiency, G6PD deficiency |
| Prevention | N/A |
| Treatment | Blood transfusion, splenectomy |
| Medication | Folic acid supplementation |
| Prognosis | Variable, depending on severity |
| Frequency | Rare |
| Deaths | N/A |
Hexokinase deficiency is a rare genetic disorder that affects the body's ability to metabolize glucose, leading to a variety of symptoms including anemia, jaundice, and fatigue. This condition is caused by mutations in the HK1 gene, which provides instructions for making an enzyme called hexokinase.
Causes[edit]
Hexokinase deficiency is caused by mutations in the HK1 gene. This gene provides instructions for making an enzyme called hexokinase, which plays a crucial role in the first step of glucose metabolism. Mutations in the HK1 gene reduce the activity of hexokinase, disrupting the normal process of glucose metabolism and leading to the symptoms of hexokinase deficiency.
Symptoms[edit]
The symptoms of hexokinase deficiency can vary widely, but they often include:
- Anemia: A condition characterized by a lack of healthy red blood cells, leading to fatigue and weakness.
- Jaundice: A yellowing of the skin and eyes, caused by a buildup of a substance called bilirubin.
- Fatigue: A feeling of tiredness or exhaustion that doesn't go away with rest.
Diagnosis[edit]
Diagnosis of hexokinase deficiency typically involves a series of tests, including blood tests to check for anemia and jaundice, and genetic testing to identify mutations in the HK1 gene.
Treatment[edit]
Treatment for hexokinase deficiency is typically focused on managing the symptoms of the condition. This can include treatments for anemia and jaundice, as well as lifestyle changes to help manage fatigue.
See also[edit]
References[edit]
<references />
